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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 821 — Medical Device Tracking Requirements
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Pt. 820
Quality Management System Regulation
Pt. 822
Postmarket Surveillance
›
Part 821 — Medical Device Tracking Requirements
Search Part 821 full text →
Subpt. A
General Provisions
§§821.1 to 821.4
Subpt. B
Tracking Requirements
§§821.20 to 821.25
Subpt. C
Additional Requirements and Responsibilities
§821.30
Subpt. D
Records and Inspections
§§821.50 to 821.60
‹
Pt. 820
Quality Management System Regulation
Pt. 822
Postmarket Surveillance
›
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