1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter H - MEDICAL DEVICES
  5. 21 CFR Part 807
21 CFR Part 807
ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES
June 25, 2020
Subpart
A
General Provisions
Subpart
B
Procedures for Device Establishments
Subpart
C
Procedures for Foreign Device Establishments
Subpart
D
Exemptions
Subpart
E
Premarket Notification Procedures
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Part 801 LABELING
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Part 806 MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS

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