FDA Authorizes First COVID-19 At-Home Sample Collection Test
The U.S. Food and Drug Administration (FDA) authorized the first at-home sample collection test for COVID-19 today.
The FDA re-issued the emergency use authorization (EUA) for LabCorp's COVID-19 RT-PCR Test, which will now be permitted to test the at-home samples people take using LabCorp's Pixel by LabCorp COVID-19 Test home collection kit.
The at-home sample collection kit includes designated nasal swabs and saline. After someone takes a sample from their nose with the special nasal swab, they mail the sample inside of an insulated package to a LabCorp lab for testing.
According to a tweet from LabCorp, kits will initially be made available to frontline healthcare workers and first responders. Kits will be available to consumers in most states, with a doctor's order, in the coming weeks, according to the FDA release.
This authorization is only for the LabCorp COVID-19 RT-PCR Test for at-home collection of nasal swab specimens using the Pixel by LabCorp COVID-19 home collection kit. This is not a general authorization for at-home COVID-19 sample collection tests.