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Home » Business, Policy & Funding » Regulatory News & FDA Approvals » FDA Emergency Use Authorization for Rheonix SARS-CoV-2 Assay Expanded to Include Saliva Samples

FDA Emergency Use Authorization for Rheonix SARS-CoV-2 Assay Expanded to Include Saliva Samples

Dec 07, 2020
|
staff reporter

NEW YORK – Molecular diagnostics instrument and assay maker Rheonix has received an expanded Emergency Use Authorization from the US Food and Drug Administration for its SARS-CoV-2 assay. The firm's test is now authorized for the use of saliva samples.

Ithaca, New York-based Rheonix obtained its initial EUA for a SARS-Cov-2 test in April.

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