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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 822
Subpart C - Subpart C—Postmarket Surveillance Plan
§ 822.8 - When, where, and how must I submit my postmarket surveillance plan?
§ 822.9 - What must I include in my submission?
§ 822.10 - What must I include in my surveillance plan?
§ 822.11 - What should I consider when designing my plan to conduct postmarket surveillance?
§ 822.12 - Do you have any information that will help me prepare my submission or design my postmarket surveillance plan?
§ 822.13 - [Reserved]
§ 822.14 - May I reference information previously submitted instead of submitting it again?
§ 822.15 - How long must I conduct postmarket surveillance of my device?
authority:
21 U.S.C. 331
,
352
,
360i
,
360l
,
371
,
374
source:
67 FR 38887, June 6, 2002, unless otherwise noted.
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