The U.S. Food and Drug Administration has issued an emergency use authorization for a new novel coronavirus test from Abbott Laboratories. Results from the speedy test come back in as little as five ...

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 ...

Demand for COVID tests has fluctuated during the course of the pandemic and Abbott has recently seen demand decline for its BinaxNOW rapid antigen tests. In the first quarter, the company reported ...

Gift Article 10 Remaining As a subscriber, you have 10 articles to gift each month. Gifting allows recipients to access the article for free. While Abbott Laboratories saw sales fall in the first ...