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 ...

The Trump administration has touted Abbott's BinaxNOW test as a quick, easy-to-use and inexpensive diagnostic that can increase the pace of U.S. COVID-19 testing at the point of care. BD, Quidel and ...

Abbott presented the data obtained from a prospective sub-study of the PARTNER trial at this year’s ASCO meeting in Chicago, ...

- 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 Laboratories said on Friday that it has received emergency use authorization from the US Food and Drug Administration for a test that can detect and differentiate COVID-19 from two types of flu ...

A medical worker wearing personal protective equipment (PPE) uses an Abbott Laboratories ID NOW rapid Covid-19 test machine at San Francisco International Airport (SFO) in San Francisco, California, U ...

Abbott has recalled two of its Alinity COVID-19 test kits after finding they can yield false positive results. Abbott is recalling its Alinity m SARS-CoV-2 AMP kit and Alinity m Resp-4-Plex AMP kit, ...

Abbott Laboratories’ sales of COVID-19 tests fell by a whopping 89% during the second quarter of this year compared with the same time last year — a drop that comes as the world attempts to move on ...

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 ...

PROVIDENCE, R.I. (WPRI) – A faulty test that Rhode Island leaders’ scientific advisers recommended phasing out months ago has re-emerged and is playing multiple roles in the state’s overall testing ...