FDA authorizes emergency use for quicker, but less reliable coronavirus antigen test

Coronavirus testing.
(Image credit: ANGELA WEISS/AFP via Getty Images)

With the United States struggling to meet the recommended quota of coronavirus tests per day, the Food and Drug Administration issued the first emergency use authorization Friday for a COVID-19 antigen test.

The test, produced by San Diego-based manufacturer Quidel, can diagnose COVID-19 by detecting fragments of protein found on or within the virus present in samples collected from the nasal cavity using swabs. The test produces results within minutes — much more quickly than many other tests on the market, which are more complex to conduct and analyze — but the technology is also more liable to result in false negatives, so an additional PCR test may be necessary to confirm.

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Tim O'Donnell

Tim is a staff writer at The Week and has contributed to Bedford and Bowery and The New York Transatlantic. He is a graduate of Occidental College and NYU's journalism school. Tim enjoys writing about baseball, Europe, and extinct megafauna. He lives in New York City.