FDA Clears First Over-the-Counter COVID-19 Antigen Test
The US Food and Drug Administration cleared for marketing the first over-the-counter antigen test for COVID-19.
The US Food and Drug Administration cleared for marketing the first over-the-counter antigen test for COVID-19.
The US FDA is warning consumers and healthcare providers to not use the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) because these tests are not authorized, cleared, or approved by the FDA.
The US FDA has authorized the BD Veritor Plus SARS-CoV-2 assay, a rapid, point-of-care, antigen test manufactured by Becton Dickinson.