Fda Authorizes First Point Of Care Antibody Test For Covid 19
The Assure COVID-19 IgG/IgM Rapid Test Device, a simple fingerstick blood test, was previously used for laboratory testing to detect antibodies to SARS-CoV-2 (the virus that causes COVID-19) in patients. The FDA explained in a press release that the EUA was re-issued to allow the test to be used in provider’s offices, hospitals, urgent care centers, and emergency rooms rather than having to be sent to a central lab for testing....