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Regulations last checked for updates: Feb 19, 2025
Title 21 - Food and Drugs last revised: Feb 03, 2025
All Titles
Title 21
Chapter I
Part 810 - PART 810—MEDICAL DEVICE RECALL AUTHORITY
Subpart A [§ 810.1 - § 810.4] - Subpart A—General Provisions
Subpart B [§ 810.10 - § 810.18] - Subpart B—Mandatory Medical Device Recall Procedures
authority:
21 U.S.C. 321
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331
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332
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333
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334
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351
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352
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355
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360h
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360i
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371
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374
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375
source:
61 FR 59018, Nov. 20, 1996, unless otherwise noted.
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