2020. 11. 18. · The FDA issued an emergency use authorization for the first COVID-19 diagnostic test that allows for self-collection and testing at home and provides test results in 30 minutes

A Covid-19 breathalyzer test with the ability to provide diagnostic results in three minutes has won emergency-use authorization from the 

2021. 7. 17. · Federal regulators revoked the authorization of a COVID-19 test that has been given to millions of people for free across the country, including hundreds of thousands in Los Angeles. The Food and

A new home test that detects COVID-19, influenza, and respiratory syncytial virus (RSV), just authorized by the FDA, will be available 

These at-home COVID-19 diagnostic tests are FDA authorized for self-testing at home (or in other locations). This means you collect your own 

Are there any FDA-approved COVID-19 antibody tests? Today, the U.S. Food and Drug Administration authorized the first serology test that detects neutralizing antibodies from recent or prior SARS-CoV-2 infection, which are antibodies that bind to a specific part of a pathogen and have been observed in a laboratory setting to decrease SARS-CoV-2 viral infection of cells.

Here's a look at which at-home COVID tests the CDC says are approved by the FDA, and how long each of the kits are good for: BinaxNOW COVID-19 Ag Card Home Test, 15 months. BinaxNOW COVID-19

The FDA released an initial version of this infographic for 2020. Text version of the infographic: COVID-19 Tests and Collection Kits Authorized by the FDA in The FDA is committed to

2022. 7. 12. · These at-home COVID-19 diagnostic tests are FDA authorized for self-testing at home (or in other locations). This means you collect your own sample, perform the test, and

While finding an appointment to get tested may be difficult right now (depending on your location), the Food and Drug Administration has authorized several at-home COVID-19 tests for emergency

2022. 3. 2. · The On/Go One™ COVID-19 Antigen Home Test has not been FDA cleared or approved but has been authorized by the FDA under an Emergency Use Authorization (EUA).