Abbott announced it has received US Food and Drug Administration (FDA) Emergency Use Authorization (EUA) for over-the-counter, non-prescription, asymptomatic use of its BinaxNOW Covid-19 Ag Self Test ...

The maker of a rapid coronavirus test widely used across the United States and distributed by the federal government has warned that its device can produce false negatives if a special solution is ...

Airport services provider, National Aviation Services (NAS) signed an agreement to partner with global healthcare company, Abbott, to drive the implementation of Covid-19 rapid testing solutions at ...

INDIANAPOLIS, (WISH) – The holidays are about spreading joy, but it’s also a time when celebrating with friends and family can get us sick. On Tuesday, Dr. Mary Rodgers, a Ph.D. who is an Abbott ...

Abbott Labs got emergency approval from the US Food and Drug Administration for its rapid antigen test, which can detect a Covid-19 infection in 15 minutes. The test is a "game changer," according to ...

Dec. 21—The company that operates a Maine factory making a widely used rapid test for COVID-19 said it would increase production by 40 percent in January amid widespread shortages of the tests before ...