SANTA CLARA, Calif., Oct. 21, 2021 /PRNewswire/ -- Xtrava Health, a health technology company, today announced the U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization ...
In a recent study published in the medRxiv* preprint server, researchers evaluated the diagnostic performance of a coronavirus disease 2019 (COVID-19) antigen test during the recent surge caused by ...
JURUPA VALLEY, Calif.--(BUSINESS WIRE)--GenBody is proud to announce that the company’s visually readable COVID-19 antigen test kit has been issued an amendment to its original Emergency Use ...
SUWON, South Korea--(BUSINESS WIRE)--SD Biosensor, Inc., a global in-vitro diagnostics company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed ...
Abbott’s BinaxNOW COVID-19 Ag Self Test, which was designed to detect COVID-19 infection, has been authorized for emergency use by the US Food and Drug Administration (FDA). The approval permits ...
(RTTNews) - Abbott Laboratories (ABT) announced Monday that it began shipping its BinaxNOW COVID-19 Ag Self Test to retailers across the country. Consumers can expect the test to be available in the ...
With cases of COVID-19 on the rise again this winter thanks in part to the new JN.1 variant of the virus, now is probably a good time to take stock of the tests you may have at home. According to data ...
The test has been authorized for home use to collect nasal swab samples from individuals 2 years of age and older. The Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) ...
BRUSSELS, Feb 18 (Reuters) - European Union officials adopted a list of COVID-19 rapid antigen tests whose results are recognised in the 27 countries of the bloc, the European Commission said on ...
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