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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 E—Responsibilities of Manufacturers

21 CFR Part 822 - Subpart E - Responsibilities of Manufacturers

  • CFR
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  1. § 822.24 What are my responsibilities once I am notified that I am required to conduct postmarket surveillance?
  2. § 822.25 What are my responsibilities after my postmarket surveillance plan has been approved?
  3. § 822.26 If my company changes ownership, what must I do?
  4. § 822.27 If I go out of business, what must I do?
  5. § 822.28 If I stop marketing the device subject to postmarket surveillance, what must I do?

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