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Tribune News Service
Tribune News Service
Lifestyle
Hanna Webster

An at-home COVID-19 and flu test gets FDA emergency use authorization

FDA Covid-19 Lucira Food and Drug Administration Influenza Lucira Health Pandemic

The Food and Drug Administration has approved an at-home test that can detect and discern between COVID-19 infection and two strains of the flu, Influenza A and B, continuing the shift from clinical to home-diagnostic care that blossomed during the height of the pandemic.

Manufactured by medical technology company Lucira Health, the test uses a nasal swab to detect the presence of a virus in 30 minutes.

The emergency use authorization, announced Friday in a news release from the Food and Drug Administration, followed a surge in respiratory cases in the fall that drove up hospitalizations nationwide and in Allegheny County. National and local respiratory cases now are trending downward.

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