Abbott Laboratories spiked 22% in Wednesday’s extended market session after announcing that the US Food and Drug Administration (FDA) issued Emergency Use Authorization (EUA) for its BinaxNOW COVID-19 ...

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 ...

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 ...

- Abbott has the most advanced and comprehensive COVID-19 rapid test portfolio available today, including ID NOW, BinaxNOW, the BinaxNOW at-home test and the NAVICA app - Workplaces, universities, ...

CHICAGO and ABBOTT PARK, Ill., May 12, 2021 – United and Abbott today announced a first-of-its-kind collaboration to use Abbott’s BinaxNOW™ COVID-19 Home Test and Abbott’s NAVICA app to help make the ...