The Food and Drug Administration granted Abbott Technologies emergency use authorization for its $5 COVID-19 antigen test Wednesday saying it's an "important addition to available tests." The test -- ...

Results are provided within 15 minutes and can be read directly from the testing card. The Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for BinaxNOW™ COVID-19 Ag ...

Today, the U.S. Food and Drug Administration issued an emergency use authorization for the first antigen test where results can be read directly from the testing card, a similar design to some ...

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 ...

Everyday Health independently vets all recommended products. If you purchase a featured product, we may be compensated. Learn why you can trust us. Everyday Health independently vets all recommended ...

The FDA has extended the shelf life for some COVID-19 tests. Now that allergy season is here, many are finding themselves with symptoms asking: Is it allergies or a cold? COVID? Something else? Since ...

According to the agency, an extended expiration date means the manufacturer provided data showing that the shelf-life is longer than was known when the test was first authorized. For more information ...

Quick and easy access to rapid COVID-19 testing felt like a pipe dream when the coronavirus pandemic first hit the U.S., but two new tests authorized by the Food and Drug Administration (FDA) are now ...

Antigen tests can identify the presence of antigens within the body, which are substances that cause immune responses, such as the release of antibodies. The immune system, and antibodies specifically ...