FDA Authorizes First At-Home COVID-19 Self Test

The U.S. Food and Drug Administration has authorized the first COVID-19 diagnostic at-home self test that provides results in 30 minutes or less. The Lucira COVID-19 All-In-One Test Kit by Lucira Health, Inc., a single-use test that is intended to detect the novel coronavirus SARS-CoV-2 that causes COVID-19, has received FDA's emergency use authorization or EUA.