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) ...
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 ...
The FDA announced the first tests for patients to collect samples at home. The FDA announced the first tests for patients to collect samples at home. The first diagnostic test with a home collection ...
Apple said today that the nasal swab company it invested in last year has shipped more than 15 million COVID collection kits across the country and increased its test-kit production by almost 4000% ...
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