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Electronic Code of Federal Regulations

e-CFR data is current as of November 12, 2019

Title 21 → Chapter I


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES

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PartTable of
Contents
Headings
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SUBCHAPTER A—GENERAL

1
1.1 to 1.980
GENERAL ENFORCEMENT REGULATIONS
2
2.5 to 2.125
GENERAL ADMINISTRATIVE RULINGS AND DECISIONS
3
3.1 to 3.10
PRODUCT JURISDICTION
4
4.1 to 4.105
REGULATION OF COMBINATION PRODUCTS
5
5.1100 to 5.1110
ORGANIZATION
7
7.1 to 7.87
ENFORCEMENT POLICY
10
10.1 to 10.206
ADMINISTRATIVE PRACTICES AND PROCEDURES
11
11.1 to 11.300
ELECTRONIC RECORDS; ELECTRONIC SIGNATURES
12
12.1 to 12.159
FORMAL EVIDENTIARY PUBLIC HEARING
13
13.1 to 13.50
PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY
14
14.1 to 14.174
PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE
15
15.1 to 15.45
PUBLIC HEARING BEFORE THE COMMISSIONER
16
16.1 to 16.120
REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION
17
17.1 to 17.54
CIVIL MONEY PENALTIES HEARINGS
19
19.1 to 19.55
STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST
20
20.1 to 20.120
PUBLIC INFORMATION
21
21.1 to 21.75
PROTECTION OF PRIVACY
25
25.1 to 25.60
ENVIRONMENTAL IMPACT CONSIDERATIONS
26
26.0 to 26.81
MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY
50
50.1 to 50.56
PROTECTION OF HUMAN SUBJECTS
54
54.1 to 54.6
FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS
56
56.101 to 56.124
INSTITUTIONAL REVIEW BOARDS
58
58.1 to 58.219
GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
60
60.1 to 60.46
PATENT TERM RESTORATION
70
70.3 to 70.55
COLOR ADDITIVES
71
71.1 to 71.37
COLOR ADDITIVE PETITIONS
73
73.1 to 73.3129
LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION
74
74.101 to 74.3710
LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION
80
80.10 to 80.39
COLOR ADDITIVE CERTIFICATION
81
81.1 to 81.32
GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS
82
82.3 to 82.2707a
LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS
83-98
[RESERVED]
99
99.1 to 99.501
DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES
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SUBCHAPTER B—FOOD FOR HUMAN CONSUMPTION

100
100.1 to 100.155
GENERAL
101
101.1 to 101.108
FOOD LABELING
102
102.5 to 102.57
COMMON OR USUAL NAME FOR NONSTANDARDIZED FOODS
104
104.5 to 104.47
NUTRITIONAL QUALITY GUIDELINES FOR FOODS
105
105.3 to 105.66
FOODS FOR SPECIAL DIETARY USE
106
106.1 to 106.160
INFANT FORMULA REQUIREMENTS PERTAINING TO CURRENT GOOD MANUFACTURING PRACTICE, QUALITY CONTROL PROCEDURES, QUALITY FACTORS, RECORDS AND REPORTS, AND NOTIFICATIONS
107
107.1 to 107.280
INFANT FORMULA
108
108.3 to 108.35
EMERGENCY PERMIT CONTROL
109
109.3 to 109.30
UNAVOIDABLE CONTAMINANTS IN FOOD FOR HUMAN CONSUMPTION AND FOOD-PACKAGING MATERIAL
110
110.3 to 110.110
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKING, OR HOLDING HUMAN FOOD
111
111.1 to 111.610
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
112
112.1 to 112.213
STANDARDS FOR THE GROWING, HARVESTING, PACKING, AND HOLDING OF PRODUCE FOR HUMAN CONSUMPTION
113
113.3 to 113.100
THERMALLY PROCESSED LOW-ACID FOODS PACKAGED IN HERMETICALLY SEALED CONTAINERS
114
114.3 to 114.100
ACIDIFIED FOODS
115
115.50
SHELL EGGS
117
117.1 to 117.475
CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD
118
118.1 to 118.12
PRODUCTION, STORAGE, AND TRANSPORTATION OF SHELL EGGS
119
119.1
DIETARY SUPPLEMENTS THAT PRESENT A SIGNIFICANT OR UNREASONABLE RISK
120
120.1 to 120.25
HAZARD ANALYSIS AND CRITICAL CONTROL POINT (HACCP) SYSTEMS
121
121.1 to 121.401
MITIGATION STRATEGIES TO PROTECT FOOD AGAINST INTENTIONAL ADULTERATION
123
123.3 to 123.28
FISH AND FISHERY PRODUCTS
129
129.1 to 129.80
PROCESSING AND BOTTLING OF BOTTLED DRINKING WATER
130
130.3 to 130.20
FOOD STANDARDS: GENERAL
131
131.3 to 131.206
MILK AND CREAM
133
133.3 to 133.196
CHEESES AND RELATED CHEESE PRODUCTS
135
135.3 to 135.160
FROZEN DESSERTS
136
136.3 to 136.180
BAKERY PRODUCTS
137
137.105 to 137.350
CEREAL FLOURS AND RELATED PRODUCTS
139
139.110 to 139.180
MACARONI AND NOODLE PRODUCTS
145
145.3 to 145.190
CANNED FRUITS
146
146.3 to 146.187
CANNED FRUIT JUICES
150
150.110 to 150.160
FRUIT BUTTERS, JELLIES, PRESERVES, AND RELATED PRODUCTS
152
152.126
FRUIT PIES
155
155.3 to 155.201
CANNED VEGETABLES
156
156.3 to 156.145
VEGETABLE JUICES
158
158.3 to 158.170
FROZEN VEGETABLES
160
160.100 to 160.190
EGGS AND EGG PRODUCTS
161
161.30 to 161.190
FISH AND SHELLFISH
163
163.5 to 163.155
CACAO PRODUCTS
164
164.110 to 164.150
TREE NUT AND PEANUT PRODUCTS
165
165.3 to 165.110
BEVERAGES
166
166.40 to 166.110
MARGARINE
168
168.110 to 168.180
SWEETENERS AND TABLE SIRUPS
169
169.3 to 169.182
FOOD DRESSINGS AND FLAVORINGS
170
170.3 to 170.285
FOOD ADDITIVES
171
171.1 to 171.130
FOOD ADDITIVE PETITIONS
172
172.5 to 172.898
FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
173
173.5 to 173.405
SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION
174
174.5 to 174.6
INDIRECT FOOD ADDITIVES: GENERAL
175
175.105 to 175.390
INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS
176
176.110 to 176.350
INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
177
177.1010 to 177.2910
INDIRECT FOOD ADDITIVES: POLYMERS
178
178.1005 to 178.3950
INDIRECT FOOD ADDITIVES: ADJUVANTS, PRODUCTION AIDS, AND SANITIZERS
179
179.21 to 179.45
IRRADIATION IN THE PRODUCTION, PROCESSING AND HANDLING OF FOOD
180
180.1 to 180.37
FOOD ADDITIVES PERMITTED IN FOOD OR IN CONTACT WITH FOOD ON AN INTERIM BASIS PENDING ADDITIONAL STUDY
181
181.1 to 181.34
PRIOR-SANCTIONED FOOD INGREDIENTS
182
182.1 to 182.8997
SUBSTANCES GENERALLY RECOGNIZED AS SAFE
184
184.1 to 184.1985
DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE
186
186.1 to 186.1839
INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE
189
189.1 to 189.301
SUBSTANCES PROHIBITED FROM USE IN HUMAN FOOD
190
190.6
DIETARY SUPPLEMENTS
191-199
[RESERVED]
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SUBCHAPTER C—DRUGS: GENERAL

200
200.5 to 200.200
GENERAL
201
201.1 to 201.328
LABELING
202
202.1
PRESCRIPTION DRUG ADVERTISING
203
203.1 to 203.70
PRESCRIPTION DRUG MARKETING
205
205.1 to 205.50
GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
206
206.1 to 206.10
IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
207
207.1 to 207.81
REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE
208
208.1 to 208.26
MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS
209
209.1 to 209.11
REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
210
210.1 to 210.3
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
211
211.1 to 211.208
CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
212
212.1 to 212.110
CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
216
216.23 to 216.24
HUMAN DRUG COMPOUNDING
225
225.1 to 225.202
CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
226
226.1 to 226.115
CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
250
250.11 to 250.250
SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
290
290.1 to 290.10
CONTROLLED DRUGS
299
299.3 to 299.5
DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES
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SUBCHAPTER D—DRUGS FOR HUMAN USE

300
300.50 to 300.100
GENERAL
310
310.3 to 310.548
NEW DRUGS
312
312.1 to 312.320
INVESTIGATIONAL NEW DRUG APPLICATION
314
314.1 to 314.650
APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG
315
315.1 to 315.6
DIAGNOSTIC RADIOPHARMACEUTICALS
316
316.1 to 316.52
ORPHAN DRUGS
317
317.1 to 317.2
QUALIFYING PATHOGENS
320
320.1 to 320.63
BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
328
328.1 to 328.50
OVER-THE-COUNTER DRUG PRODUCTS INTENDED FOR ORAL INGESTION THAT CONTAIN ALCOHOL
329
329.100
NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
330
330.1 to 330.15
OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED
331
331.1 to 331.80
ANTACID PRODUCTS FOR OVER-THE-COUNTER (OTC) HUMAN USE
332
332.1 to 332.31
ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
333
333.101 to 333.350
TOPICAL ANTIMICROBIAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
335
335.1 to 335.50
ANTIDIARRHEAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
336
336.1 to 336.80
ANTIEMETIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
338
338.1 to 338.50
NIGHTTIME SLEEP-AID DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
340
340.1 to 340.50
STIMULANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
341
341.1 to 341.90
COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
343
343.1 to 343.90
INTERNAL ANALGESIC, ANTIPYRETIC, AND ANTIRHEUMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
344
344.1 to 344.52
TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
346
346.1 to 346.52
ANORECTAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
347
347.1 to 347.60
SKIN PROTECTANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
348
348.1 to 348.50
EXTERNAL ANALGESIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
349
349.1 to 349.80
OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
350
350.1 to 350.60
ANTIPERSPIRANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
352
352.1 to 352.77
SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]
355
355.1 to 355.70
ANTICARIES DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
357
357.101 to 357.850
MISCELLANEOUS INTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
358
358.101 to 358.760
MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
361
361.1
PRESCRIPTION DRUGS FOR HUMAN USE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED: DRUGS USED IN RESEARCH
369
369.1 to 369.21
INTERPRETATIVE STATEMENTS RE WARNINGS ON DRUGS AND DEVICES FOR OVER-THE-COUNTER SALE
370-499
[RESERVED]
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SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS

500
500.23 to 500.1410
GENERAL
501
501.1 to 501.110
ANIMAL FOOD LABELING
502
502.5 to 502.19
COMMON OR USUAL NAMES FOR NONSTANDARDIZED ANIMAL FOODS
507
507.1 to 507.215
CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR FOOD FOR ANIMALS
509
509.3 to 509.30
UNAVOIDABLE CONTAMINANTS IN ANIMAL FOOD AND FOOD-PACKAGING MATERIAL
510
510.3 to 510.600
NEW ANIMAL DRUGS
511
511.1 to 511.3
NEW ANIMAL DRUGS FOR INVESTIGATIONAL USE
514
514.1 to 514.235
NEW ANIMAL DRUG APPLICATIONS
515
515.10 to 515.40
MEDICATED FEED MILL LICENSE
516
516.1 to 516.2065
NEW ANIMAL DRUGS FOR MINOR USE AND MINOR SPECIES
520
520.23 to 520.2645
ORAL DOSAGE FORM NEW ANIMAL DRUGS
522
522.23 to 522.2690
IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS
524
524.86 to 524.2620
OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS
526
526.88 to 526.1810
INTRAMAMMARY DOSAGE FORM NEW ANIMAL DRUGS
528
528.1070 to 528.2010
NEW ANIMAL DRUGS IN GENETICALLY ENGINEERED ANIMALS
529
529.40 to 529.2620
CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS
530
530.1 to 530.41
EXTRALABEL DRUG USE IN ANIMALS
556
556.1 to 556.770
TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
558
558.3 to 558.680
NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS
564
[RESERVED]
570
570.3 to 570.280
FOOD ADDITIVES
571
571.1 to 571.130
FOOD ADDITIVE PETITIONS
573
573.120 to 573.1020
FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS
579
579.12 to 579.40
IRRADIATION IN THE PRODUCTION, PROCESSING, AND HANDLING OF ANIMAL FEED AND PET FOOD
582
582.1 to 582.7724
SUBSTANCES GENERALLY RECOGNIZED AS SAFE
584
584.200 to 584.725
FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE IN FEED AND DRINKING WATER OF ANIMALS
589
589.1 to 589.2001
SUBSTANCES PROHIBITED FROM USE IN ANIMAL FOOD OR FEED
590-599
[RESERVED]
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SUBCHAPTER F—BIOLOGICS

600
600.2 to 600.90
BIOLOGICAL PRODUCTS: GENERAL
601
601.2 to 601.95
LICENSING
606
606.3 to 606.171
CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
607
607.1 to 607.80
ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
610
610.1 to 610.68
GENERAL BIOLOGICAL PRODUCTS STANDARDS
630
630.1 to 630.40
REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE
640
640.1 to 640.130
ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
660
660.1 to 660.55
ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS
680
680.1 to 680.3
ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS
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SUBCHAPTER G—COSMETICS

700
700.3 to 700.35
GENERAL
701
701.1 to 701.30
COSMETIC LABELING
710
710.1 to 710.9
VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS
720
720.1 to 720.9
VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS
740
740.1 to 740.19
COSMETIC PRODUCT WARNING STATEMENTS
741-799
[RESERVED]
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SUBCHAPTER H—MEDICAL DEVICES

800
800.10 to 800.75
GENERAL
801
801.1 to 801.437
LABELING
803
803.1 to 803.58
MEDICAL DEVICE REPORTING
806
806.1 to 806.40
MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
807
807.3 to 807.100
ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
808
808.1 to 808.101
EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
809
809.3 to 809.40
IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
810
810.1 to 810.18
MEDICAL DEVICE RECALL AUTHORITY
812
812.1 to 812.150
INVESTIGATIONAL DEVICE EXEMPTIONS
813
[RESERVED]
814
814.1 to 814.126
PREMARKET APPROVAL OF MEDICAL DEVICES
820
820.1 to 820.250
QUALITY SYSTEM REGULATION
821
821.1 to 821.60
MEDICAL DEVICE TRACKING REQUIREMENTS
822
822.1 to 822.38
POSTMARKET SURVEILLANCE
830
830.3 to 830.360
UNIQUE DEVICE IDENTIFICATION
860
860.1 to 860.136
MEDICAL DEVICE CLASSIFICATION PROCEDURES
861
861.1 to 861.38
PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
862
862.1 to 862.3950
CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
864
864.1 to 864.9900
HEMATOLOGY AND PATHOLOGY DEVICES
866
866.1 to 866.6080
IMMUNOLOGY AND MICROBIOLOGY DEVICES
868
868.1 to 868.6885
ANESTHESIOLOGY DEVICES
870
870.1 to 870.5925
CARDIOVASCULAR DEVICES
872
872.1 to 872.6890
DENTAL DEVICES
874
874.1 to 874.5900
EAR, NOSE, AND THROAT DEVICES
876
876.1 to 876.5990
GASTROENTEROLOGY-UROLOGY DEVICES
878
878.1 to 878.5910
GENERAL AND PLASTIC SURGERY DEVICES
880
880.1 to 880.6992
GENERAL HOSPITAL AND PERSONAL USE DEVICES
882
882.1 to 882.5975
NEUROLOGICAL DEVICES
884
884.1 to 884.6200
OBSTETRICAL AND GYNECOLOGICAL DEVICES
886
886.1 to 886.5933
OPHTHALMIC DEVICES
888
888.1 to 888.5980
ORTHOPEDIC DEVICES
890
890.1 to 890.5975
PHYSICAL MEDICINE DEVICES
892
892.1 to 892.6500
RADIOLOGY DEVICES
895
895.1 to 895.104
BANNED DEVICES
898
898.11 to 898.14
PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
rule

SUBCHAPTER I—MAMMOGRAPHY QUALITY STANDARDS ACT

900
900.1 to 900.25
MAMMOGRAPHY
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SUBCHAPTER J—RADIOLOGICAL HEALTH

1000
1000.1 to 1000.60
GENERAL
1002
1002.1 to 1002.51
RECORDS AND REPORTS
1003
1003.1 to 1003.31
NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
1004
1004.1 to 1004.6
REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
1005
1005.1 to 1005.25
IMPORTATION OF ELECTRONIC PRODUCTS
1010
1010.1 to 1010.20
PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
1020
1020.10 to 1020.40
PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
1030
1030.10
PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
1040
1040.10 to 1040.30
PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
1050
1050.10
PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
rule

SUBCHAPTER K—TOBACCO PRODUCTS

1100
1100.1 to 1100.5
TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY
1105
1105.10
GENERAL
1107
1107.1
ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
1140
1140.1 to 1140.34
CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS
1141
1141.1 to 1141.16
CIGARETTE PACKAGE AND ADVERTISING WARNINGS
1143
1143.1 to 1143.13
MINIMUM REQUIRED WARNING STATEMENTS
1150
1150.1 to 1150.17
USER FEES
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SUBCHAPTER L—REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION

1210
1210.1 to 1210.31
REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
1230
1230.2 to 1230.49
REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
1240
1240.3 to 1240.95
CONTROL OF COMMUNICABLE DISEASES
1250
1250.3 to 1250.96
INTERSTATE CONVEYANCE SANITATION
1251-1269
[RESERVED]
1270
1270.1 to 1270.43
HUMAN TISSUE INTENDED FOR TRANSPLANTATION
1271
1271.1 to 1271.440
HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
1272-1299
[RESERVED]

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