The Food and Drug Administration has issued an emergency use authorization for the Lucira COVID-19 All-In-One Test Kit, the first rapid test to detect the COVID-19 virus that one can administer completely at home when prescribed by a health care provider to individuals age 14 or older. Previously authorized at-home test kits allow the user to collect a sample at home and send it to a lab for testing.
The authorization letter can be obtained at https://www.fda.gov/media/143810/download.