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The United States has approved the first rapid test for Covid-19, which is used in emergency situations and can be performed alone, at a time when restrictions are mounting across the country to reduce the increase in HIV infections.
The Food and Drug Administration has approved the test for people 14 years of age and older that a doctor suspects have COVID-19. The conditional prescription test shows results within 30 minutes.
“We continue to demonstrate unprecedented speed in responding to Covid-19,” wrote FDA Commissioner Stephen Hahn in a tweet, adding, “The Food and Drug Administration has approved the first COVID-19 test which is completely self-administered and provides results at home. Scope of access for testing. “
The test is developed by Lucera Health. It is allowed to take nasal samples at home using an attached swab, which is then placed in a small package and then placed in a small device that examines the sample. A light flashes on the device that displays the test result in 30 minutes or less.
The test is designed to cost less than $ 50, according to Lucera Health.
The United States Food and Drug Administration had previously approved home testing for Covid-19, and in late April and early May it gave two tests taking samples from the nose and another test for saliva samples, but the samples taken from these tests were sent to a laboratory for examination. Instead of checking it out at home.
While the Lucera test provides results immediately, it’s not the type of quick, cheap test that researchers have advocated for widespread use.
The United States recorded 11,340,563 emerging coronavirus cases and 248,429 deaths on Tuesday, according to the Johns Hopkins Center. Both results are the worst in the world.
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