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 ...

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.

Abbott Laboratories has been given the greenlight by the Food and Drug Administration for an emergency use authorization for its $5 rapid antigen test for the coronavirus. The test, called the ...

- 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 ...

Just as controversial new recommendations on coronavirus testing arrive from the CDC, the FDA has granted emergency use authorization (PDF) to another rapid COVID-19 testing setup from Abbott. The ...

Today, the U.S. Food and Drug Administration issued a new emergency use authorization (EUA) for the BinaxNOW COVID-19 Ag Card Home Test which is authorized for use by patients at home with a ...

Editor's note: Find the latest COVID-19 news and guidance in Medscape's Coronavirus Resource Center. The BinaxNOW COVID-19 Ag Card (Abbott) rapid antigen test for SARS-CoV-2 can now be used at home ...

With no vaccine much less a cure in sight yet, the best that healthcare systems can do to fight the COVID-19 coronavirus is to treat infected people and isolate them immediately. That, however, ...

Abbott Laboratories won Food and Drug Administration emergency clearance for its portable test for the coronavirus strain Covid-19 that will sell for just $5 and allow for “frequent mass testing” in ...

A COVID-19 test that takes 15 minutes and can be run without lab equipment was just granted emergency use authorization by the Food and Drug Administration. It will cost $5, and runs on a simple card ...