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C.F.R. Title 21 Chapter I Subchapter H Part 803

Code of Federal Regulations · Part

Part 803 — Medical Device Reporting

21 C.F.R. pt. 803

  • Subpart A General Provisions
  • Subpart B Generally Applicable Requirements For Individual Adverse Event Reports
  • Subpart C User Facility Reporting Requirements
  • Subpart D Importer Reporting Requirements
  • Subpart E Manufacturer Reporting Requirements
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