Regulations.gov document

Authorization of Emergency Use of an In Vitro Diagnostic Device in Response to an Outbreak…

Notice · FDA-2023-N-0249 · posted Jul 5, 2024

Key facts

Document ID FDA-2023-N-0249-0003
Title Authorization of Emergency Use of an In Vitro Diagnostic Device in Response to an Outbreak of Mpox; Availability
Document type Notice
Subtype General Notice
Agency FDA
Docket FDA-2023-N-0249
Posted Jul 5, 2024
Federal Register citation 89 FR 55615
FR document number 2024-14719
Effective date Jul 5, 2024

At a glance

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

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