Abbott's AdviseDx SARS-CoV-2 IgM Test Receives the US FDA's EUA for COVID-19
Shots:
- Abbott has received the US FDA’s EUA for AdviseDx SARS-CoV-2 IgM lab-based serology test for use on the ARCHITECT and Alinity platforms
- Till now- Abbott has received EUA for its seven tests- including molecular tests- a rapid antigen test and- an IgG Ab test for COVID-19
- The IgM test demonstrated 99.56% specificity and 95.00% sensitivity for patients tested 15 days after symptom onset. The test will give a more complete picture of where patients are in their recovery
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