Regulations.gov document

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

Notice · FDA-2022-N-0150 · posted May 29, 2025

Key facts

Document ID FDA-2022-N-0150-0015
Title Revocation of Four 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 May 29, 2025
Federal Register citation 90 FR 22727
FR document number 2025-09678
Comment period opens May 29, 2025
Effective date May 29, 2025

At a glance

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

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