- 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 announced that the US Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for virtually guided at-home use of its BinaxNOW COVID-19 Ag Card rapid test for detection ...

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 ...

According to a statement from ODH, "results of at-home tests provided by the state are reported on the COVID-19 dashboard. The tests are conducted in a guided manner through a virtual appointment, and ...

The Food and Drug Administration (FDA) on Wednesday granted emergency use authorization for the cheapest at-home COVID-19 test yet, but consumers will need a prescription to obtain one. The BinaxNOW ...

Abbott Laboratories has been granted Emergency Use Authorization (EUA) by the US Food and Drug Administration (FDA) for its virtually guided at-home BinaxNow COVID-19 Ag Card rapid test. Abbott (ABT) ...

ABBOTT PARK, Ill.,, Dec. 16, 2020 /PRNewswire/ -- Abbott (NYSE: ABT) announced today that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for virtually guided ...