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Electronic Code of Federal Regulations

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e-CFR data is current as of May 5, 2021

Title 21Chapter ISubchapter JPart 1002Subpart A → §1002.1

Title 21: Food and Drugs
Subpart A—General Provisions

§1002.1   Applicability.

The provisions of this part are applicable as follows:

(a) All manufacturers of electronic products are subject to §1002.20.

(b) Manufacturers, dealers, and distributors of electronic products are subject to the provisions of part 1002 as set forth in table 1 of this section, unless excluded by paragraph (c) of this section, or unless an exemption has been granted under §1002.50 or §1002.51.

(c) The requirements of part 1002 as specified in table 1 of this section are not applicable to:

(1) Manufacturers of electronic products intended solely for export if such product is labeled or tagged to show that the product meets all the applicable requirements of the country to which such product is intended for export.

(2) Manufacturers of electronic products listed in table 1 of this section if such product is sold exclusively to other manufacturers for use as components of electronic products to be sold to purchasers, with the exception that the provisions are applicable to those manufacturers certifying components of diagnostic x-ray systems pursuant to provisions of §1020.30(c) of this chapter.

(3) Manufacturers of electronic products that are intended for use by the U.S. Government and whose function or design cannot be divulged by the manufacturer for reasons of national security, as evidenced by government security classification.

(4) Assemblers of diagnostic x-ray equipment subject to the provisions of §1020.30(d) of this chapter, provided the assembler has submitted the report required by §1020.30(d)(1) or (d)(2) of this chapter and retains a copy of such report for a period of 5 years from its date.

Table 1—Record and Reporting Requirements By Product

ManufacturerDealer & Distributor
ProductsProduct reports §1002.10Supplemental reports §1002.11Abbreviated reports §1002.12Annual reports §1002.13Test records §1002.30(a)1Distribution records §1002.30(b)2Distribution records §§1002.40 and 1002.41
DIAGNOSTIC X-RAY3 (1020.30, 1020.31, 1020.32, 1020.33)
Computed tomographyXXXXXX
X-ray system4XXXXXX
Tube housing assemblyXXXXX
X-ray controlXXXXXX
X-ray high voltage generatorXXXXXX
X-ray table or cradleXXXX
X-ray film changerXXX
Vertical cassette holders mounted in a fixed location and cassette holders with front panelsXXXX
Beam-limiting devicesXXXXXX
Spot-film devices and image intensifiers manufactured after April 26, 1977XXXXXX
Cephalometric devices manufactured after February 25, 1978XXX
Image receptor support devices for mammographic X-ray systems manufactured after September 5, 1978XXXX
CABINET X RAY (§1020.40)
Baggage inspectionXXXXXX
<25 kilovolt (kV) and <0.1 milliroentgen per hour (mR/hr IRLC5 6XX6
≥25kV and <0.1mR/hr IRLC5XXX
≥0.1mR/hr IRLC5XXXXX
MW ovens (§1030.10)XXXXX
MW diathermyX
MW heating, drying, security systemsX
RF sealers, electromagnetic induction and heating equipment, dielectric heaters (2-500 megahertz)X
Phototherapy productsXX
Laser products (§§1040.10, 1040.11)
Class I lasers and products containing such lasers7XXX
Class I laser products containing class IIa, II, IIIa, lasers7XXXX
Class IIa, II, IIIa lasers and products other than class I products containing such lasers7XXXXXX
Class IIIb and IV lasers and products containing such lasers7XXXXXX
Sunlamp products (§1040.20)
Lamps onlyX
Sunlamp productsXXXXXX
Mercury vapor lamps (§1040.30)
T lampsXXX
R lampsX
Ultrasonic therapy (1050.10)XXXXXX
Diagnostic ultrasoundX
Medical ultrasound other than therapy or diagnosticXX
Nonmedical ultrasoundX

1However, authority to inspect all appropriate documents supporting the adequacy of a manufacturer's compliance testing program is retained.

2The requirement includes §§1002.31 and 1002.42, if applicable.

3Report of Assembly (Form FDA 2579) is required for diagnostic x-ray components; see 21 CFR 1020.30(d)(1) through (d)(3).

4Systems records and reports are required if a manufacturer exercises the option and certifies the system as permitted in 21 CFR 1020.30(c).

5Determined using the isoexposure rate limit curve (IRLC) under phase III test conditions (1020.10(c)(3)(iii)).

6Annual report is for production status information only.

7Determination of the applicable reporting category for a laser product shall be based on the worst-case hazard present within the laser product.

[60 FR 48382, Sept. 19, 1995; 61 FR 13423, Mar. 27, 1996]

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