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 BinaxNOWâ„¢ COVID-19 Ag ...
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 -- ...
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 ...
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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 ...
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 ...
For instance, if you only get a very faint line, it might be hard to know whether or not that means your results are positive. I know how that feels firsthand. After more than two years of evading ...
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 ...
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