BD received 510(k) clearance for COVID-19, influenza A/B, RSV molecular combination test

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On Aug. 1, 2023, BD announced that the U.S. Food and Drug Administration (FDA) 510(k) had provided clearance for the BD Respiratory Viral Panel (RVP) for BD MAXル System, a single molecular diagnostic combination test that identifies and distinguishes SARS-CoV-2, influenza A, influenza B, and Respiratory Syncytial Virus (RSV) in approximately two hours.

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Source: Becton, Dickinson and Company
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