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Code of Federal Regulations
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Title 21
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Chapter I — Food and Drug Administration, Department of Health and Human Services
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Subchapter H — Medical Devices
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Part 807 — Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
‹
Pt. 806
Medical Devices; Reports of Corrections and Removals
Pt. 808
Exemptions from Federal Preemption of State and Local Medical Device Requirements
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Part 807 — Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
Search Part 807 full text →
Subpt. A
General Provisions
§807.3
Subpt. B
Procedures for Device Establishments
§§807.20 to 807.39
Subpt. C
Procedures for Foreign Device Establishments
§§807.40 to 807.41
Subpt. D
Exemptions
§807.65
Subpt. E
Premarket Notification Procedures
§§807.81 to 807.100
‹
Pt. 806
Medical Devices; Reports of Corrections and Removals
Pt. 808
Exemptions from Federal Preemption of State and Local Medical Device Requirements
›
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