Regulations.gov document

Revocation of Three Authorizations of Emergency Use of In Vitro Diagnostic Devices for…

Notice · FDA-2022-N-0150 · posted Mar 20, 2025

Key facts

Document ID FDA-2022-N-0150-0014
Title Revocation of Three Authorizations of Emergency Use of In Vitro Diagnostic Devices for Detection and/or Diagnosis of COVID–19; Availability
Document type Notice
Subtype Announcement
Agency FDA
Docket FDA-2022-N-0150
Posted Mar 20, 2025
Federal Register citation 90 FR 13164
FR document number 2025-04710
Effective date Mar 20, 2025

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  • 1–9 Pages
  • None Public comments on this docket

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