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Mesa Biotech Receives EUA from FDA

Palm-sized testing system will enable broader use across healthcare facilities closer to the patients and will begin shipping immediately

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By: TOM BRANNA

Chief Content Officer

Mesa Biotech has received Emergency Use Authorization (EUA) from the U.S. Food & Drug Administration (FDA) for its Accula SARS-CoV-2 Test, which gives COVID-19 diagnostic results in 30 minutes. Mesa Biotech, a privately-held, molecular diagnostic company has developed the testing platform designed for point-of-care (POC) infectious disease diagnosis. The COVID-19 test uses this patented technology to enable ‘near patient’ testing allowing testing outside of the central laboratory...

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