(Reuters) - The U.S. Food and Drug Administration said on Thursday that Abbott Laboratories’ speedy coronavirus test, which can deliver results within minutes and is used at the White House, could ...
Abbott said Oct. 12 it has received emergency authorization from the FDA for a new antibody test that is designed to detect more recent infections. The AdviseDx test can detect a COVID-19 antibody ...
The test, run on Abbott's portable i-STAT® Alinity® instrument, uses whole blood to help evaluate patients with a suspected mild traumatic brain injury (mTBI), or concussion The test produces ...
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