FDA Grants Third Emergency-Use Authorization For H7N9 Flu Test

The April 25 emergency authorization covers the use of Arbor Vita Corp.’s rapid H7N9 assay in government laboratories on U.S. citizens who are suspected of exposure to the variant of avian flu in China.

FDA granted emergency use authorization on April 25 to a rapid diagnostic for use in government laboratories to help detect the H7N9 variant of avian flu in U.S. citizens who have traveled to China.

The authorization, for Fremont, Calif.-based Arbor Vita Corp.’srapid H7N9 assay, is the third emergency authorization granted by FDA for a diagnostic targeting this strain since it was officially deemed...

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