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 ...
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 ...
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 ...
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 ...
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% ...
Last May, Apple’s Advanced Manufacturing Fund awarded $10 million to COPAN Diagnostics to accelerate its supply of sample kits for hospitals across the U.S., expand production and help the expansion ...
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