Depending on the COVID -19 rapid test , the expiration date may have been extended beyond what's listed on the package. Here's how to find out the right date. China rapid testing kit, rapid test kit factory, visit here to find the at home rapid test kit, rapid kit test that you are searching for. Select Language. English.

The FDA still recommends going to the doctor if you have serious symptoms or are concerned about possible exposure to Covid. However, the latest 

2021. 11. 1. · KANSAS CITY, Mo. — The United States Food and Drug Administration (FDA) approved its first at-home COVID-19 test in November , and has authorized at least 400 additional tests and collection

People are receiving expired COVID-19 test kits. Published: Sep. 14, 2022 at 8:32 PM PDT. The FDA extended the shelf life for more than half of the approved test kits beyond their printed

2022. 3. 14. · FDA. The company made the announcement about the other Flowflex tests in January, and the FDA published it on Friday. There've been no reports of adverse events, but because the duplicate tests

2021. 12. 25. · Roche announced Friday that the Food and Drug Administration has granted its at-home COVID-19 test emergency use authorization. The test, which uses a nasal swab sample, can produce “accurate

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

Molecular SARS-CoV-2 Diagnostic Tests for COVID-19 that have been granted a De Novo, 510 (k) clearance or PMA BioFire Respiratory Panel 2.1 (RP2.1) - On March 17, , FDA granted the first

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

The FDA has issued an emergency use authorization for the SalivaDirect COVID-19 diagnostic test, developed by the Yale School of Public 

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