Breaking news: USFDA approves Point-of-Care Test that can detect Novel Coronavirus in 5 mins
USA: The U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) to Abbott's molecular point-of-care test can detect novel coronavirus (COVID-19) positive cases in as little as five minutes.
Abbott announced today that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for the fastest available molecular point-of-care test for the detection of novel coronavirus (COVID-19), delivering positive results in as little as five minutes and negative results in 13 minutes. The test will run on the company's ID NOW™ platform, providing rapid results in a wide range of healthcare settings such as physicians' offices, urgent care clinics and hospital emergency departments.
Testing is being performed on Abbott's ID NOW platform.
ID NOW test components are being made in Abbott's U.S. manufacturing facility
The ID NOW platform is small, lightweight (6.6 pounds) and portable (the size of a small toaster), and uses molecular technology, which is valued by clinicians and the scientific community for its high degree of accuracy. ID NOW is already the most widely available molecular point-of-care testing platform in the U.S. today.
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