FDA grants first emergency use ok for at-home COVID-19 test

US Food and Drug Administration has granted an emergency use authorization for the first time to a COVID-19 diagnostic test that people can use at home.

Lucira Health, the company that makes the test, announced on Wednesday that the 30-minute diagnostic will be available by prescription only.

Read: https://cen.acs.org/analytical-chemistry/diagnostics/FDA-grants-first-emergency-use-ok-for-at-home-COVID-19-test/98/web/2020/11