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  • Abbott Receives EUA for COVID-19 IgM Antibody Blood Test americanpharmaceuticalreview
    October 16, 2020
    Abbott announced the U.S. Food and Drug Administration (FDA) issued Emergency Use Authorization (EUA) for the company's AdviseDx SARS-CoV-2 IgM (Immunoglobulin M) lab-based serology test for use on the ARCHITECT® and Alinity™ platforms.

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