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March 05, 2021 10:56 AM

Abbott gets emergency use authorization for test that detects COVID-19, other infections

GenomeWeb
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    Modern Healthcare Illustration / Getty Images

    NEW YORK — Abbott said on Friday that it has received Emergency Use Authorization from the US Food and Drug Administration for a PCR-based assay that can detect and differentiate SARS-CoV-2, influenza A, influenza B, and respiratory syncytial virus.

    The newly authorized Alinity m Resp-4-Plex assay uses a single anterior nasal or nasopharyngeal swab sample collected by a healthcare provider or self-collected at a healthcare facility, according to Abbott. It runs on the company's Alinity m system.

    Abbott also said that the previously granted EUA for its Alinity m SARS-CoV-2 test has been updated to include its use with asymptomatic individuals, as well as with pooled samples.

    That test was first authorized by the FDA in December for detecting SARS-CoV-2 nucleic acid in nasal, nasopharyngeal, and oropharyngeal swabs, as well as bronchoalveolar lavage specimens, collected from individuals suspected of having COVID-19.

    According to Abbott Park, Illinois-based Abbott, that EUA has now been expanded to allow the test's use with people not showing symptoms of infection and with up to five samples at a time.

    This article originally appeared in Modern Healthcare's sister publication GenomeWeb.

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        • Midwest
        • Northeast
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