Friday, August 28, 2020

First rapid COVID-19 (New Coronavirus Infection) The trial, which does not require special computer equipment to produce results, was approved by the US Food and Drug Administration on Wednesday.

The 15-minute test created by Abbott Laboratories sells for $ 5 and is superior to similar tests that need to be inserted into a small machine. Associated Press report. Credit Cards The Abbott test below is based on the same technology used for the test. influenza, Streptococcal pharyngitis, And other infectious diseases. BinaxNOW is the fourth rapid test detected in the United States. COVID-19 (New Coronavirus Infection) Antigen, not the virus itself. This is considered a faster, but less accurate screening method.

Abbott’s rapid entry COVID-19 (New Coronavirus Infection) The test market offers yet another option for extending your tests. The FDA recently approved a saliva test from Yale University. This bypasses some of the supply that led to the inspection bottleneck. AP report. Neither test can be run at home. Abbott’s new test, like most older people, requires healthcare professionals to collect nasal swabs. COVID-19 (New Coronavirus Infection) test. Yale saliva testing eliminates the need for cotton swabs, but can only be performed in high-quality laboratories. Since the pandemic began, nasal swab tests sent to the lab have been COVID-19 (New Coronavirus Infection) Sifting. The tests are believed to be very accurate, but rely on expensive, specialized machinery and chemicals. According to the news agency, the shortage of these supplies has repeatedly delayed reporting of the results.

Currently, about 690,000 Americans are taking daily tests from the peak of 850,000 daily tests at the end of last month. AP report. However, many public health professionals have reopened schools and influenza The season is coming.

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FDA-approved rapid 15-minute COVID-19 test

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