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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER H—MEDICAL DEVICES
  6. PART 822—POSTMARKET SURVEILLANCE
  7. Subpart C—Postmarket Surveillance Plan

21 CFR Part 822 - Subpart C - Postmarket Surveillance Plan

  • CFR
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  1. § 822.8 When, where, and how must I submit my postmarket surveillance plan?
  2. § 822.9 What must I include in my submission?
  3. § 822.10 What must I include in my surveillance plan?
  4. § 822.11 What should I consider when designing my plan to conduct postmarket surveillance?
  5. § 822.12 Do you have any information that will help me prepare my submission or design my postmarket surveillance plan?
  6. § 822.13 [Reserved]
  7. § 822.14 May I reference information previously submitted instead of submitting it again?
  8. § 822.15 How long must I conduct postmarket surveillance of my device?

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