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 ...
COVID-19 cases in the U.S. nearly quadrupled over the summer, rising by more than 6.2 million cases between Memorial Day weekend and Sept. 8. according to data tracked by The Washington Post. The ...
For the first time, the FDA has authorized coronavirus tests that can be sold directly to Americans who do not have to go through a health care provider. An emergency use authorization is not a full ...
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 ...
March 5 (Reuters) - Diagnostics company Laboratory Corp of America Holdings said on Thursday it will make its coronavirus test available for ordering by healthcare providers from 6 p.m. ET, as the U.S ...
(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 ...
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