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FDA grants EUA to Acon Laboratories’ Covid-19 antigen home test

October 5, 2021

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The US Food and Drug Administration (FDA) has granted emergency use authorization (EUA) to Acon Laboratories’ Flowflex COVID-19 Antigen Home Test.

Flowflex is an over the counter (OTC) antigen test, which uses nasal swab specimens from individuals suspected of active Covid-19.

Individuals aged 14 years and above can use the new home test for self-testing. It can also be used for children aged two years or older with nasal swabs collected by adults.

Read More on medicaldevice-network.com