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FDA grants emergency use authorisation for Abbott’s Covid-19 test

March 19, 2020

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The US Food and Drug Administration (FDA) has granted emergency use authorisation (EUA) for Abbott’s molecular test for coronavirus (Covid-19).

The molecular tests are run on the company’s m2000 RealTime System, a molecular solution with a broad range of tests.

Following the EUA, Abbott is shipping 150,000 RealTime SARS-CoV-2 tests to existing customers in the US.

Abbott chairman and CEO Miles White said: “A global challenge like coronavirus requires the commitment and cooperation of everyone who has the ability to help address it.

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