Home » Xtrava’s Spera COVID-19 Test Gets FDA’s Emergency Use Authorization
Xtrava’s Spera COVID-19 Test Gets FDA’s Emergency Use Authorization
Santa Clara, Calif.-based Xtrava Health has received the FDA’s Emergency Use Authorization (EUA) for its COVID-19 antigen test, dubbed the Spera COVID-19 Ag Test.
The test uses immunochromatographic technology to detect SARS-CoV-2 nucleocapsid protein in anterior nasal swab specimens.
The EUA covers the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus in direct anterior nasal swabs from individuals suspected of COVID-19 by their healthcare provider within the first five days of symptoms.
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