Free Republic

The Food and Drug Administration has approved the first at-home test for the coronavirus. It's made by LabCorp, that said due to limited quantities, it will first be made available to healthcare workers and first responders... The FDA approval is not a "general authorization for at-home collection of patient samples" and only applies to the LabCorp testing kit. Right now, the kits are available in Maryland, New Jersey, New York and Rhode Island.

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 Emergency Use Authorization for LabCorp to COVID-19 RT-PCR Test to permit testing of samples that were self-collected by patients at home using LabCorp's Pixel by LabCorp COVID-19 Test home collection kit. "Throughout this pandemic we have been facilitating test development to ensure patients access to accurate diagnostics, which includes supporting the development of reliable and accurate at-home sample collection options," said FDA Commissioner Dr. Stephen Hahn.