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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 809 — In Vitro Diagnostic Products for Human Use
‹
Pt. 808
Exemptions from Federal Preemption of State and Local Medical Device Requirements
Pt. 810
Medical Device Recall Authority
›
Part 809 — In Vitro Diagnostic Products for Human Use
Search Part 809 full text →
Subpt. A
General Provisions
§§809.3 to 809.4
Subpt. B
Labeling
§§809.10 to 809.11
Subpt. C
Requirements for Manufacturers and Producers
§§809.20 to 809.40
‹
Pt. 808
Exemptions from Federal Preemption of State and Local Medical Device Requirements
Pt. 810
Medical Device Recall Authority
›
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