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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 B—Notification

21 CFR Part 822 - Subpart B - Notification

  • CFR
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  1. § 822.5 How will I know if I must conduct postmarket surveillance?
  2. § 822.6 When will you notify me that I am required to conduct postmarket surveillance?
  3. § 822.7 What should I do if I do not agree that postmarket surveillance is appropriate?

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