BURLINGTON, North Carolina -- LabCorp has received emergency use authorization from the Food and Drug Administration for its Pixel at home coronavirus test kit. The COVID-19 At Home Test Kit allows ...

The FDA has authorized the first diagnostic test with a home collection option for COVID-19, the disease caused by coronavirus. In a statement released Tuesday, the FDA said that it had reissued an ...

LabCorp's $119 at-home testing kits are currently limited in supply. But it plans on selling them to consumers in the coming weeks. When he's not battling bugs and robots in Helldivers 2, Michael is ...

North Carolina’s LabCorp has gotten the federal go-ahead for an at-home testing kit for COVID-19, the new coronavirus. It’s the first authorized by the Food and Drug Administration. LabCorp of ...

The FDA has granted emergency approval use for a coronavirus test that can be conducted by patients at their homes. The FDA re-issued emergency use approval for the Pixel by LabCorp COVID-19 home ...

LabCorp on Tuesday announced the launch of the first testing method to simultaneously detect for COVID-19, influenza A / B, and respiratory syncytial virus (RSV) ahead of flu season. CDC tells states: ...

(Reuters) - LabCorp said on Thursday it has launched a new test that could assess the capacity of antibodies in patient plasma to inhibit the novel coronavirus. Information from the test about the ...

Add Yahoo as a preferred source to see more of our stories on Google. an iHealth COVID-19 antigen rapid test kit The federal government may destroy its remaining supply of COVID-19 tests. The US ...