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