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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Aug 27, 2025
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Title 21
Chapter I
Part 803 - PART 803—MEDICAL DEVICE REPORTING
Subpart A [§ 803.1 - § 803.19] - Subpart A—General Provisions
Subpart B [§ 803.20 - § 803.23] - Subpart B—Generally Applicable Requirements for Individual Adverse Event Reports
Subpart C [§ 803.30 - § 803.33] - Subpart C—User Facility Reporting Requirements
Subpart D [§ 803.40 - § 803.42] - Subpart D—Importer Reporting Requirements
Subpart E [§ 803.50 - § 803.58] - Subpart E—Manufacturer Reporting Requirements
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