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FDA Issues EUA for Ebola Diagnostic

04/22/2016

Federal Register Notice: FDA is issuing an Emergency Use Authorization for an in vitro diagnostic device for detecting the Ebola Zaire virus in response to the Ebola virus outbreak in West Africa. The authorization was requested by OraSure Technologies and contains, among other things, conditions on the emergency use of the authorized in vitro diagnostic device. To view this notice, click here.

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