US Codex
C.F.R.
Legal Codes
United States Code
U.S.C.
Federal statutory law
Code of Federal Regulations
C.F.R.
Federal administrative regulations (eCFR)
Public Laws
Pub. L.
Enacted acts of Congress (113th onward)
Congressional Bills
Bill
Proposed and enacted legislation (113th Congress onward)
Executive Orders
E.O.
Presidential executive orders (2000 onward)
Browse by date
View an earlier version
Go
Latest
Current
1 year ago
Sep 3, 2025
5 years ago
Sep 3, 2021
Browse all versions by date
Notes
Notes
Browse by date
Home
About
Data
Privacy
MCP
…
/
Code of Federal Regulations
/
Title 21
/
Chapter I — Food and Drug Administration, Department of Health and Human Services
/
Subchapter H — Medical Devices
/
Part 821 — Medical Device Tracking Requirements
‹
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
›
Add note
Incoming references
Copy permalink
Cite
Cite this provision
×
Format
Bluebook
ALWD
APA
MLA
Include provision text
Copy citation
Incoming references
×