FDA approves new at-home rapid COVID-19 test
by Virginia Aabram, Breaking News Reporter
December 30, 2021 11:19 AMThe Food and Drug Administration has granted emergency use authorization to a new at-home rapid COVID-19 test manufactured by Siemens Healthineers.
The German-American company's at-home test was approved by the agency Wednesday amid a coronavirus testing shortage as cases surge across the country. Siemens Healthineers said it expects to provide "tens of millions" of tests each month beginning in January.
“Undetected COVID-19 exposure is a major driver of community spread. With the CLINITEST Rapid COVID-19 Antigen Self-Test, consumers will have access to a fast, reliable, and convenient test to provide additional safety,” said Christoph Pedain, head of point of care diagnostics, in a statement. “Siemens Healthineers is proud to bring this high-quality test, already used and trusted by families, medical professionals, businesses and governments in many parts of the world, to the United States under FDA emergency use authorization.”
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https://www.washingtonexaminer.com/news/fda-approves-new-at-home-rapid-covid-19-test