CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER H—MEDICAL DEVICES > PART 810—MEDICAL DEVICE RECALL AUTHORITY" /> 21 CFR Part 810 - MEDICAL DEVICE RECALL AUTHORITY | Electronic Code of Federal Regulations (e-CFR) | US Law | LII / Legal Information Institute

21 CFR Part 810 - MEDICAL DEVICE RECALL AUTHORITY

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Subpart A—General Provisions (§§ 810.1 - 810.4)
Subpart B—Mandatory Medical Device Recall Procedures (§§ 810.10 - 810.18)

Authority:

21 U.S.C. 321, 331, 332, 333, 334, 351, 352, 355, 360h, 360i, 371, 374, 375.

Source:

61 FR 59018, Nov. 20, 1996, unless otherwise noted.