Federal Register: FDA Issues Notice on Availability of Emergency Use Authorization for Mpox Diagnostic Device
August 06, 2026
August 06, 2026
WASHINGTON, Aug. 6 (TNSFR) -- The U.S. Department of Health and Human Services Food and Drug Administration issued the following action in the Federal Register.
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The Food and Drug Administration (FDA) is announcing the issuance of an Emergency Use Authorization (EUA) under the Federal Food, Drug, and Cosmetic Act in response to an outbreak of Mpox. FDA has issued an Authorization for an in vitro diagnostic device, Allplex HSV-1&2/VZV/MPXV Assay, for the simulta . . .
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The Food and Drug Administration (FDA) is announcing the issuance of an Emergency Use Authorization (EUA) under the Federal Food, Drug, and Cosmetic Act in response to an outbreak of Mpox. FDA has issued an Authorization for an in vitro diagnostic device, Allplex HSV-1&2/VZV/MPXV Assay, for the simulta . . .