FDA approves 5-minute coronavirus test by Abbott Labs

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FDA approves 5-minute coronavirus test by Abbott Labs
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Abbott Laboratories is unveiling a coronavirus test that can tell if someone is infected in as little as five minutes, and is so small and portable it can be used in almost any healthcare setting.

The medical-device maker plans to supply 50,000 tests a day starting Wednesday, said John Frels, vice president of research and development at Abbott Diagnostics.

Abbott has received emergency use authorization from the U.S. Food and Drug Administration “for use by authorized laboratories and patient care settings,” the companyThe U.S. has struggled to supply enough tests to detect the virus, even as the outbreak threatens to overwhelm hospitals in New York, California, Washington and other areas. After initially restricting testing to high-risk people, and problems with a test designed by the Centers for Disease Control and Prevention, U.S.

The technology builds on Illinois-based Abbott’s ID Now platform, the most common point-of-care test currently available in the U.S., with more than 18,000 units spread across the country. It is widely used to detect influenza, strep throat and respiratory syncytial virus, a common bug that causes cold-like symptoms.

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