§810.1. Scope.
21 C.F.R. § 810.1
Part 810 describes the procedures that the Food and Drug Administration will follow in exercising its medical device recall authority under section 518(e) of the Federal Food, Drug, and Cosmetic Act.
Notes, amendments, and revision history
Authority
Authority: 21 U.S.C. 321, 331, 332, 333, 334, 351, 352, 355, 360h, 360i, 371, 374, 375.
Source
Source: 61 FR 59018, Nov. 20, 1996, unless otherwise noted.