Regulations.gov document

Authorization of Emergency Use of Two In Vitro Diagnostic Devices in Response to an…

Notice · FDA-2023-N-0249 · posted Jan 31, 2023

Key facts

Document ID FDA-2023-N-0249-0001
Title Authorization of Emergency Use of Two In Vitro Diagnostic Devices in Response to an Outbreak of Mpox; Availability
Document type Notice
Subtype Announcement
Agency FDA
Docket FDA-2023-N-0249
Posted Jan 31, 2023
Federal Register citation 88 FR 6262
FR document number 2023-01987
Comment period opens Jan 31, 2023
Effective date Jan 31, 2023

At a glance

  • 10–99 Pages
  • None Public comments on this docket

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