www.fdanews.com/articles/196445-abbotts-15-minute-covid-19-test-authorized-for-emergency-use
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Abbott’s 15-Minute COVID-19 Test Authorized for Emergency Use
March 30, 2020
The FDA granted an Emergency Use Authorization to Abbot Laboratories’ point-of-care COVID-19 test that can deliver results in less than 15 minutes.
The rapid molecular point-of-care test delivers positive COVID-19 results in five minutes and negative results in 13 minutes.
The test will run on Abbott’s portable ID NOW platform, which is the most widely-available point-of-care-testing platform in the U.S.