Tuesday, May 12, 2020

FDA approves fast-results antigen test for COVID-19

The Food and Drug Administration on Friday issued emergency use authorization for the Sofia 2 SARS Antigen FIA made by Quidel Corporation. Like an in-office flu test, the diagnostic is administered using a nasal swab. Results are processed on proprietary instruments and can be available in 15 minutes, according to the San Diego-based manufacturer.McNights

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