[Code of Federal Regulations] [Title 21, Volume 8] [Revised as of April 1, 2002] From the U.S. Government Printing Office via GPO Access [CITE: 21CFR1002.1] [Page 569-571] TITLE 21--FOOD AND DRUGS CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) PART 1002--RECORDS AND REPORTS--Table of Contents Subpart A--General Provisions Sec. 1002.1 Applicability. The provisions of this part are applicable as follows: (a) All manufacturers of electronic products are subject to Sec. 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 Sec. 1002.50 or Sec. 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 Sec. 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 Sec. 1020.30(d) of this chapter, provided the assembler has submitted the report required by Sec. 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. [[Page 570]] Table 1--Record and Reporting Requirements By Product ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ Manufacturer Dealer & ----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- Distributor ------------- Product Supplemental Abbreviated Annual Distribution Distribution Products reports Sec. reports Sec. reports Sec. reports Sec. Test records Sec. records Sec. records 1002.10 1002.11 1002.12 1002.13 1002.30(a)1 1002.30(b)2 1002.40 and 1002.41 ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ DIAGNOSTIC X-RAY3(1020.30, 1020.31, 1020.32, 1020.33) .............. ............. ............. ............. ................. ................. ............ Computed tomography X X ............. X X X X X-ray system4 X X ............. X X X X Tube housing assembly X X ............. X X X ............ X-ray control X X ............. X X X X X-ray high voltage generator X X ............. X X X X X-ray table or cradle .............. ............. X ............. X X X X-ray film changer .............. ............. X ............. X X ............ Vertical cassette holders mounted in a fixed location and cassette holders with .............. ............. X ............. X X X front panels Beam-limiting devices X X ............. X X X X Spot-film devices and image intensifiers manufactured after April 26, 1977 X X ............. X X X X Cephalometric devices manufactured after February 25, 1978 .............. ............. X ............. X X ............ Image receptor support devices for mammographic X-ray systems manufactured .............. ............. X ............. X X X after September 5, 1978 CABINET X RAY (Sec. 1020.40) .............. ............. ............. ............. ................. ................. ............ Baggage inspection X X ............. X X X X Other X X ............. X X X ............ PRODUCTS INTENDED TO PRODUCE PARTICULATE RADIATION OR X-RAYS OTHER THAN .............. ............. ............. ............. ................. ................. ............ DIAGNOSTIC OR CABINET DIAGNOSTIC X-RAY Medical .............. ............. X X X X ............ Analytical .............. ............. X X X X ............ Industrial .............. ............. X X X X ............ TELEVISION PRODUCTS (Sec. 1020.10) .............. ............. ............. ............. ................. ................. ............ <25 kilovolt (kV) and <0.1 milliroentgen per hour (mR/hr IRLC5,6 .............. ............. X X6 ................. ................. ............ [gteqt]25kV and <0.1mR/hr IRLC5 X X ............. X ................. ................. ............ [gteqt]0.1mR/hr IRLC5 X X ............. X X X ............ MICROWAVE/RF .............. ............. ............. ............. ................. ................. ............ MW ovens (Sec. 1030.10) X X ............. X X X ............ MW diathermy .............. ............. X ............. ................. ................. ............ MW heating, drying, security systems .............. ............. X ............. ................. ................. ............ RF sealers, electromagnetic induction and heating equipment, dielectric heaters .............. ............. X ............. ................. ................. ............ (2-500 megahertz) OPTICAL .............. ............. ............. ............. ................. ................. ............ Phototherapy products X X ............. ............. ................. ................. ............ Laser products (Secs. 1040.10, 1040.11) .............. ............. ............. ............. ................. ................. ............ Class I lasers and products containing such lasers7 X ............. ............. X X ................. ............ Class I laser products containing class IIa, II, IIIa, lasers7 X ............. ............. X X X ............ Class IIa, II, IIIa lasers and products other than class I products containing X X ............. X X X X such lasers7 Class IIIb and IV lasers and products containing such lasers7 X X ............. X X X X [[Page 571]] Sunlamp products (Sec. 1040.20) .............. ............. ............. ............. ................. ................. ............ Lamps only X ............. ............. ............. ................. ................. ............ Sunlamp products X X ............. X X X X Mercury vapor lamps (Sec. 1040.30) .............. ............. ............. ............. ................. ................. ............ T lamps X X ............. X ................. ................. ............ R lamps .............. ............. X ............. ................. ................. ............ ACOUSTIC .............. ............. ............. ............. ................. ................. ............ Ultrasonic therapy (1050.10) X X ............. X X X X Diagnostic ultrasound .............. ............. X ............. ................. ................. ............ Medical ultrasound other than therapy or diagnostic X X ............. ............. ................. ................. ............ Nonmedical ultrasound .............. ............. X ............. ................. ................. ............ ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ \1\However, authority to inspect all appropriate documents supporting the adequacy of a manufacturer's compliance testing program is retained. \2\The requirement includes Secs. 1002.31 and 1002.42, if applicable. \3\Report of Assembly (Form FDA 2579) is required for diagnostic x-ray components; see 21 CFR 1020.30(d)(1) through (d)(3). \4\Systems records and reports are required if a manufacturer exercises the option and certifies the system as permitted in 21 CFR 1020.30(c). \5\Determined using the isoexposure rate limit curve (IRLC) under phase III test conditions (1020.10(c)(3)(iii)). \6\Annual report is for production status information only. \7\Determination 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] [[Page 572]]