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.
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.
Pero bien, interesante
Mmmmm ya no creo en nada que tenga que ver con covid-19, mira es vacuna como esta causando infartos y pérdida de memoria
Waoo que buen avance en la medicina
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