COVID-19 Update: FDA Continues to Advance Over-the Counter and Other Screening Test Development On March 31, the U.S. Food and Drug Administration (FDA) authorized several COVID-19 tests for over-the-counter (OTC) use without a prescription when used for serial screening (testing asymptomatic individuals multiple times on a routine basis), such as testing twice a week in schools or other settings. The FDA also authorized serial screening tests for use in a point-of-care (POC) setting, such as a doctor's office. These authorizations follow the FDA's recent actions to advance OTC and other screening test development. These tests: - Can be used to test people with or without COVID-19 symptoms.
- Are antigen tests that detect proteins from SARS-CoV-2, the virus that causes COVID-19, from a nasal swab sample.
- Give results in 10-30 minutes without needing to send a sample to a laboratory for analysis.
Specific tests authorized yesterday: - Quidel QuickVue At-Home OTC COVID-19 test - authorized for OTC at-home serial screening
- Abbott BinaxNOW (multiple configurations)
- Abbott BinaxNOW COVID-19 Antigen Self Test - authorized for OTC at-home serial screening
- Abbott BinaxNOW COVID-19 Ag Card 2 Home Test - authorized for OTC at-home serial screening with telehealth proctor
- Abbott BinaxNOW COVID-19 Ag 2 Card - authorized for POC serial screening without a prescription
- BD Veritor System for Rapid Detection of SARS-CoV-2 - authorized for POC serial screening with a prescription
Questions? If you have questions, email COVID19DX@fda.hhs.gov. |
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