The U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first COVID-19 diagnostic test for self-testing at home and that provides rapid results. The Lucira COVID-19 All-In-One Test Kit intended to detect the novel coronavirus SARS-CoV-2 that causes COVID-19. While COVID-19 diagnostic tests have been authorized for at-home collection, this is …
Tag: US Food & Drug Administration
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