US approves first rapid home Covid-19 test
The US issued an emergency use authorization for the first self-administered rapid coronavirus test Tuesday, as more parts of the country increase restrictions in an attempt to halt a Covid-19 surge.
The Food and Drug Administration approved a testing kit for people age 14 and older whom a doctor suspects to have Covid-19. The test, which is by prescription only, delivers results in 30 minutes.
"We continue to demonstrate unprecedented speed in response to #COVID19," tweeted FDA commissioner Stephen Hahn.
"FDA authorized the first #COVID19 test that's fully self-administered & provides results at home. It's an important advancement, underscoring our commitment to expanding test access."
Comments