WASHINGTON -- The head of the Food and Drug Administration said Friday his agency has provided new guidance to the White House after data suggested that a rapid COVID-19 test used by President Donald ...
The Food and Drug Administration on Wednesday announced that it has authorized Abbott Labs' rapid Covid-19 test for at-home use, though doctors must prescribe the test for patients. It's the third ...
Abbott Laboratories said Wednesday it received federal emergency use authorization for its in-home rapid COVID-19 test, with results available in 15 minutes. The north suburban-based medical device ...
ABBOTT PARK, Ill., March 31, 2021 /PRNewswire/ -- Abbott (NYSE: ABT) announced today it has received U.S. Food and Drug Administration (FDA) Emergency Use Authorization (EUA) for over-the-counter, non ...
Abbott Laboratories in August won Food and Drug Administration emergency clearance for its portable test for the coronavirus strain Covid-19 that sells for just $5 and allow for “frequent mass testing ...
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