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  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i7
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 822
    PART 822—POSTMARKET SURVEILLANCE
  5. subpart C
    Subpart C—Postmarket Surveillance Plan

Subpart C. Subpart C—Postmarket Surveillance Plan

  • § 822.8 -
  • § 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?
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