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HHS - 21 CFR PART 810

MEDICAL DEVICE RECALL AUTHORITY

active, Most Current
Organization: HHS
Publication Date: 1 April 2014
Status: active
Page Count: 8
scope:

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.

Document History

April 1, 2020
MEDICAL DEVICE RECALL AUTHORITY
810.1 Scope. 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...
April 1, 2019
MEDICAL DEVICE RECALL AUTHORITY
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.
April 1, 2018
MEDICAL DEVICE RECALL AUTHORITY
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.
April 1, 2017
MEDICAL DEVICE RECALL AUTHORITY
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.
April 1, 2016
MEDICAL DEVICE RECALL AUTHORITY
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.
April 1, 2015
MEDICAL DEVICE RECALL AUTHORITY
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.
21 CFR PART 810
April 1, 2014
MEDICAL DEVICE RECALL AUTHORITY
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.
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