FDA authorizes rapid $5 coronavirus test that doesn't need specialty equipment

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FDA authorizes rapid $5 coronavirus test that doesn't need specialty equipment
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The Food and Drug Administration on Wednesday authorized the first rapid coronavirus test that doesn’t need any special computer equipment to get results.

Doctors at Harbor-UCLA are participating in a COVID-19 vaccine trial, and they’re aiming to recruit people of color and members of other high-risk groups.

Government and health experts view rapid tests that can be run outside the laboratory system as key to boosting capacity.“Those screening tests are what we need in schools, workplaces and nursing homes in order to catch asymptomatic spreaders,” saidof the Rockefeller Foundation in an interview this month. The nonprofit group has called for the U.S. to conduct about 4 millions per day by October, mostly rapid, point-of-care tests.

Inside the Abbott test is a specially coated strip that interacts with COVID-19 antigens. The patient’s nasal swab is inserted into the card and a few drops of a chemical solution are added. Markings appear on the card to indicate whether the sample is positive or negative — much like a pregnancy test.

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