La Administración de Drogas y Alimentos de EE. UU. (FDA) aprobó este viernes la primera prueba en el hogar que puede indicar a los usuarios si tienen gripe y/o COVID-19.
La prueba, llevada a cabo por la empresa de biotecnología de California Lucira Health, utiliza un hisopo nasal único y puede proporcionar resultados en aproximadamente media hora.
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La prueba se puede comprar sin receta médica. Está autorizado para que cualquier persona de 14 años en adelante lo recoja por sí mismo, o un adulto puede dárselo a un niño de 2 años o más.
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Waoo que buen avance en la medicina
Mmmmm ya no creo en nada que tenga que ver con covid-19, mira es vacuna como esta causando infartos y pérdida de memoria
Pero bien, interesante