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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 810 — Medical Device Recall Authority
‹
Pt. 809
In Vitro Diagnostic Products for Human Use
Pt. 812
Investigational Device Exemptions
›
Part 810 — Medical Device Recall Authority
Search Part 810 full text →
Subpt. A
General Provisions
§§810.1 to 810.4
Subpt. B
Mandatory Medical Device Recall Procedures
§§810.10 to 810.18
‹
Pt. 809
In Vitro Diagnostic Products for Human Use
Pt. 812
Investigational Device Exemptions
›
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