C.F.R. » Title 21 » 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

21 C.F.R. § 810.1

Scope

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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 of Decisions
Cited in 1 case, 2016–2016 · leading case: Stevens v. Boston Sci. Corp., 152 F. Supp. 3d 527 (S.D.W. Va 2016).
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Stevens v. Boston Sci. Corp., 152 F. Supp. 3d 527 (S.D.W. Va 2016). “21 C.F.R. § 810.1 , et seq. . 21 C.F.R. § 821.”
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