CFR > Title 21 - Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES (parts 800 to 898) > PART 809—IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE > SUBPART C—Requirements for Manufacturers and Producers (§809.20 to §809.40) > 809.20—General requirements for manufacturers and producers of in vitro diagnostic products.

809.20—General requirements for manufacturers and producers of in vitro diagnostic products.

(a) [Reserved]
(b) Compliance with good manufacturing practices. In vitro diagnostic products shall be manufactured in accordance with the good manufacturing practices requirements found in part 820 of this chapter and, if applicable, with § 610.44 of this chapter.

Code of Federal Regulations

[41 FR 6903, Feb. 13, 1976, as amended at 42 FR 42530, Aug. 23, 1977; 43 FR 31527, July 21, 1978; 66 FR 31165, June 11, 2001]