EVANSTON, Ill.--(BUSINESS WIRE)--Minute Molecular Diagnostics today announced that the U.S. Food and Drug Administration (FDA) granted an Emergency Use Authorization (EUA) for its rapid DASH ...

This FDA EUA first and only PCR quality, single-use, COVID-19 at home, self-test kit is available for $55 to all Amazon US customers EMERYVILLE, Calif.--(BUSINESS WIRE)--Lucira Health, Inc. (Nasdaq: ...

NEW YORK CITY (WABC) -- It could be a game changer in COVID 19 testing: A company with offices in the Tri-State area received emergency authorization from the FDA for a test that could get results ...

SANTA BARBARA, Calif., Feb. 24, 2025 /PRNewswire/ — Aptitude Medical Systems, Inc. (Aptitude) today announced it has received Emergency Use Authorization (EUA) from the U.S. Food and Drug ...

EMERYVILLE, Calif., Jan. 03, 2023 (GLOBE NEWSWIRE) -- Lucira Health, Inc. (LHDX) ("Lucira Health" or "Lucira"), a medical technology company, announced that it submitted an Emergency Use Authorization ...

The FDA has issued its first emergency use authorization for a COVID-19 molecular diagnostic test that does not require a prescription and can be used at home. Developed by Cue Health, the Cue ...

There have been a variety of recent updates and advances in COVID-19 testing and analysis methods. The FDA Says: Check for COVID-19 Test Expiration Date Extensions The US Food and Drug Administration ...

Finland's Nokia on Thursday reported a stronger than expected 38% rise in fourth-quarter adjusted operating profit helped by higher sales of telecom equipment to mobile operators in North America and ...

SAN DIEGO — Flu season is right around the corner in San Diego, and many people are searching for quicker, easier ways to find out if they’re sick. At-home COVID testing became popular a few years ago ...

One day, long COVID in children could be objectively diagnosed with a blood test, thanks to the help of artificial intelligence (AI). In fact, a study by the Università Cattolica del Sacro Cuore, Rome ...