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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 810—MEDICAL DEVICE RECALL AUTHORITY
  7. Subpart B—Mandatory Medical Device Recall Procedures

21 CFR Part 810 - Subpart B - Mandatory Medical Device Recall Procedures

  • CFR
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  1. § 810.10 Cease distribution and notification order.
  2. § 810.11 Regulatory hearing.
  3. § 810.12 Written request for review of cease distribution and notification order.
  4. § 810.13 Mandatory recall order.
  5. § 810.14 Cease distribution and notification or mandatory recall strategy.
  6. § 810.15 Communications concerning a cease distribution and notification or mandatory recall order.
  7. § 810.16 Cease distribution and notification or mandatory recall order status reports.
  8. § 810.17 Termination of a cease distribution and notification or mandatory recall order.
  9. § 810.18 Public notice.

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