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Electronic Code of Federal Regulations
| e-CFR data is current as of April 2, 2020
TITLE 21—Food and Drugs
CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) SUBCHAPTER H—MEDICAL DEVICES 
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| MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
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| ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
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| EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS
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| IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE
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| MEDICAL DEVICE RECALL AUTHORITY
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| INVESTIGATIONAL DEVICE EXEMPTIONS
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| PREMARKET APPROVAL OF MEDICAL DEVICES
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| QUALITY SYSTEM REGULATION
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| MEDICAL DEVICE TRACKING REQUIREMENTS
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| UNIQUE DEVICE IDENTIFICATION
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| MEDICAL DEVICE CLASSIFICATION PROCEDURES
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| PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT
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| CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES
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| HEMATOLOGY AND PATHOLOGY DEVICES
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| IMMUNOLOGY AND MICROBIOLOGY DEVICES
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| EAR, NOSE, AND THROAT DEVICES
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| GASTROENTEROLOGY-UROLOGY DEVICES
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| GENERAL AND PLASTIC SURGERY DEVICES
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| GENERAL HOSPITAL AND PERSONAL USE DEVICES
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| OBSTETRICAL AND GYNECOLOGICAL DEVICES
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| PHYSICAL MEDICINE DEVICES
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| PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES
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SUBCHAPTER I—MAMMOGRAPHY QUALITY STANDARDS ACT
SUBCHAPTER J—RADIOLOGICAL HEALTH
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| NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY
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| REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS
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| IMPORTATION OF ELECTRONIC PRODUCTS
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| PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL
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| PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS
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| PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS
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| PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS
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| PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS
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SUBCHAPTER K—TOBACCO PRODUCTS
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| TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY
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| ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS
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| CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS
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| CIGARETTE PACKAGE AND ADVERTISING WARNINGS
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| MINIMUM REQUIRED WARNING STATEMENTS
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SUBCHAPTER L—REGULATIONS UNDER CERTAIN OTHER ACTS ADMINISTERED BY THE FOOD AND DRUG ADMINISTRATION
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| REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT
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| REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT
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| CONTROL OF COMMUNICABLE DISEASES
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| INTERSTATE CONVEYANCE SANITATION
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| HUMAN TISSUE INTENDED FOR TRANSPLANTATION
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| HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS
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