- First at-home, virtually guided service to bring rapid, reliable and affordable testing into the home where the result is delivered in minutes - Abbott and eMed™ expect to deliver and administer 30 ...

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 ...

BinaxNow is a hugely popular COVID-19 test kit that quickly became a preferred choice at the height of the pandemic. The tests detect 84.6% of positive COVID-19 cases and 98.5% of negative cases, ...

Quick and easy access to rapid COVID-19 testing felt like a pipe dream when the coronavirus pandemic first hit the U.S., but two new tests authorized by the Food and Drug Administration (FDA) are now ...

New, rapid COVID-19 testing supplies will be distributed to some Massachusetts schools by early December, Massachusetts health and education officials announced Wednesday. Materials will be ...

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 ...

To avoid contamination, first wash your hands and avoid contact with testing surfaces. 2. Add drops Then for the BinaxNOW kit, put six drops from the dropper bottle into the top hole of the card. 3.

CNN medical correspondent Elizabeth Cohen reported the at-home BinaxNOW antigen test will be wrong 35% of the time if you have COVID with symptoms and will be wrong 64% of the time if you have COVID ...

Baker-Polito Administration announced the distribution of the first round of Abbott BinaxNOW tests from the federal government that has been prioritized for use in K-12 schools providing in-person ...

The Abbott BinaxNOW, a rapid antigen test, identified 95 percent of people carrying high levels of the virus, researchers found. By Emily Anthes The Abbott BinaxNOW, a widely used at-home coronavirus ...