FDA Webview
X

Free FDA Notices

FDA Issues EUA for Zika Diagnostic

04/22/2016

Federal Register Notice: FDA is issuing an Emergency Use Authorization for an in vitro diagnostic device for detecting Zika virus in response to the Zika virus outbreak in the Americas. It contains, among other things, conditions on the emergency use of the authorized in vitro diagnostic device. To view this notice, click here.

LATEST NEWS