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 ...

FDA Emergency Use Authorization permits asymptomatic, non-prescription, over-the-counter self use for people with or without symptoms The BinaxNOW COVID-19 Self Test is identical to the ...

DISTRICTS OF MASSACHUSETTS HAVE CAREFULLY IMPLEMENTED SOUND HEALTH PROTOCOLS DEVELOPED BY MD PH IN CONSULTATION WITH MEDICAL EXPERTS. THESE APPEAR TO HAVE HAD A ...

Shortly after Abbott completed its delivery of 150 million rapid antigen tests to the federal government for widespread distribution against the COVID-19 pandemic, researchers at the Centers for ...

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 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 ...

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 ...