GroundRules
21 CFR 810.1: Scope.
Where this section sits in the code
- Title 21—Food and Drugs
- CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER H—MEDICAL DEVICES
- PART 810—MEDICAL DEVICE RECALL AUTHORITY
- Subpart A—General Provisions
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.
Collected 2026-08-27T02:24:47Z. Source file · JSON