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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 808 — Exemptions from Federal Preemption of State and Local Medical Device Requirements
‹
Pt. 807
Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
Pt. 809
In Vitro Diagnostic Products for Human Use
›
Part 808 — Exemptions from Federal Preemption of State and Local Medical Device Requirements
Search Part 808 full text →
Subpt. A
General Provisions
§§808.1 to 808.5
Subpt. B
Exemption Procedures
§§808.20 to 808.35
Subpt. C
Listing of Specific State and Local Exemptions
§§808.53 to 808.57-808.101
‹
Pt. 807
Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices
Pt. 809
In Vitro Diagnostic Products for Human Use
›
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