FDA Gives Abbott Emergency Use of Five-Minute Coronavirus Test

The machine can be run in doctor’s offices and other point-of-care settings to give rapid results.

Written byKerry Grens
| 2 min read
coronavirus covid-19 sars-cov-2 test assay analysis point-of-care swab id now abbott labs mesa biotech cepheid fda emergency use authorization

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ABOVE: ABBOTT

The US Food and Drug Administration has granted emergency use authorization of Abbott’s newest coronavirus test, which can read out positive results within 5 minutes and negative results in 13 minutes. The portable ID NOW machine, which will run the SARS-CoV-2 test, can be used in doctor’s offices, expanding the availability of testing beyond hospital and laboratory settings, and the company aims to produce 50,000 tests daily starting next week.

The FDA has given emergency use authorization (EUA) to other point-of-care coronavirus tests, namely, Cepheid’s 45-minute assay and Mesa Biotech’s 30-minute test. As STAT reported, Cepheid’s test would be applied in urgent situations, say, to help with triaging patients, rather than in doctor’s offices. Mesa’s instrument, like Abbott’s, can be used in doctor’s offices, nursing facilities, and elsewhere.

COVID-19 diagnoses have topped 140,000 in the US and deaths have surpassed 2,400, according to the Centers for Disease Control ...

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Meet the Author

  • kerry grens

    Kerry served as The Scientist’s news director until 2021. Before joining The Scientist in 2013, she was a stringer for Reuters Health, the senior health and science reporter at WHYY in Philadelphia, and the health and science reporter at New Hampshire Public Radio. Kerry got her start in journalism as a AAAS Mass Media fellow at KUNC in Colorado. She has a master’s in biological sciences from Stanford University and a biology degree from Loyola University Chicago.

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