FDA issued new authorization for the BinaxNOW COVID-19 Ag Card Home Test

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On Dec. 16, 2020, the U.S. Food and Drug Administration issued a new emergency use authorization (EUA) for the BinaxNOW COVID-19 Ag Card Home Test which is authorized for use by patients at home with a prescription.

The BinaxNOW COVID-19 Ag Card Home Test was authorized for prescription use at home with self-collected nasal swab samples from individuals ages 15 years or older who are suspected of COVID-19 by their healthcare provider within the first seven days of symptom onset.

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Source: U.S. Food and Drug Administration
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