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Abbott's fast, $5, 15-minute, easy-to-use COVID-19 antigen test receives FDA Emergency Use Approval
Abbott (NYSE: ABT) announced that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for its BinaxNOW™ COVID…
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Abbott gets US FDA emergency use authorization for COVID-19 molecular test on new Alinity m system | Pharma News
Abbott, a global healthcare leader, announced that the US Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the …
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