May 9 (Reuters) - The U.S. Food and Drug Administration (FDA) on Saturday approved emergency use authorization (EUA) to Quidel Corp for the first COVID-19 antigen test.
The emergency use authorization was issued late Friday to Quidel for the Sofia 2 SARS Antigen FIA, the agency said.
The FDA said the authorization is for an antigen test, which is a new type of diagnostic test designed for rapid detection of the virus that causes COVID-19.
The FDA on Friday also authorized the first diagnostic test for the new coronavirus that allows patients to collect saliva samples at home. (Reporting by Sabahatjahan Contractor in Bengaluru; editing by Diane Craft)
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