PP_1170x120_10-25-21

Ellume COVID-19 Home Test

FDA authorizes antigen test as first O-T-C fully at-home diagnostic test for COVID-19

FDA authorizes antigen test as first O-T-C fully at-home diagnostic test for COVID-19

WASHINGTON — The U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first over-the-counter (O-T-C) fully at-home diagnostic test for COVID-19. The Ellume COVID-19 Home Test is a rapid, lateral flow antigen test, a type of test that runs a liquid sample along a surface with reactive molecules. The test detects fragments