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[![Abbott rapid COVID-19 antigen test](https://blog.abclonal.com/hubfs/rsz_1abbott_binaxnow_test.jpg)](https://blog.abclonal.com/blog/covid-19-development-fda-oks-abbott-rapid-antigen-test)

 Sep 17, 2020, 12:00:00 PM       by [Dennis Miao](https://blog.abclonal.com/blog/author/dennis-miao)

## [FDA OKs Abbott's COVID-19 Rapid Test Kit](https://blog.abclonal.com/blog/covid-19-development-fda-oks-abbott-rapid-antigen-test)

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In a [press release on August 26th, 2020](https://abbott.mediaroom.com/2020-08-26-Abbotts-Fast-5-15-Minute-Easy-to-Use-COVID-19-Antigen-Test-Receives-FDA-Emergency-Use-Authorization-Mobile-App-Displays-Test-Results-to-Help-Our-Return-to-Daily-Life-Ramping-Production-to-50-Million-Tests-a-Month), Abbott Laboratories announced that they were issued an emergency use authorization (EUA) by the FDA for their new, rapid point-of-care COVID-19 antigen test. Branded as the “BinaxNOW COVID-19 Ag Card”, the test is unique compared to the more prevalent molecular-based detection tests for COVID-19 in that it utilizes a [lateral flow assay](https://en.wikipedia.org/wiki/Lateral_flow_test), similar to traditional over-the-counter pregnancy tests. Contained in a portable, credit-card sized device, Abbott claims that the test can deliver results in as little as 15 minutes, representing a significant reduction in time compared to RT-PCR-based tests that have turnaround times on a scale of hours rather than minutes.

 

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