WASHINGTON, D.C. – The Food and Drug Administration announced Saturday that it has authorized an at-home sample collection kit that can then be sent to specified laboratories for COVID-19 diagnostic ...
FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection The US Food and Drug Administration (FDA) on Friday granted the first emergency use authorization (EUA) ...
Money comes from Apple's Advanced Manufacturing Fund. Apple is awarding $10 million from its Advanced Manufacturing Fund to COPAN Diagnostics, a company making sample collection kits for COVID-19 ...
The US Food and Drug Administration (FDA) on Tuesday granted an emergency use authorization (EUA) to LabCorp allowing it to test self-collected nasal swab samples from patients for coronavirus disease ...
ITHACA, N.Y.--(BUSINESS WIRE)--Rheonix Inc. announced today that the United States Food and Drug Administration (FDA) has issued an expanded Emergency Use Authorization (EUA) for the Rheonix COVID-19™ ...
OMAHA, Neb.--(BUSINESS WIRE)--University Medical Devices (UMD), a cutting-edge healthcare technology developer, today announced the launch of its first specimen collection method, MicroWash. Developed ...
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