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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 820 — Quality Management System Regulation
‹
Pt. 814
Premarket Approval of Medical Devices
Pt. 821
Medical Device Tracking Requirements
›
Part 820 — Quality Management System Regulation
Search Part 820 full text →
Subpt. A
General Provisions
§§820.1 to 820.10
Subpt. B
Supplemental Provisions
§§820.20-820.30 to 820.45
Subpt. C-O
Subparts C-O [Reserved]
‹
Pt. 814
Premarket Approval of Medical Devices
Pt. 821
Medical Device Tracking Requirements
›
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