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# KorvaLabs Covid Test EUA Revoked
- URL: https://www.fdaweb.com/korvalabs-covid-test-eua-revoked/
- Published: 2021-07-16T12:00:00.000Z
- Updated: 2026-09-14T17:06:36.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5149729

KorvaLabs has requested that its [emergency use authorization](https://www.fda.gov/media/137089/download?ref=fdaweb.com) for the Curative SARS-Cov-2 (Covid-19) test be revoked because it is now using different EUA-authorized tests for the testing offered at its laboratories. The Curative test was the subject of a January FDA [safety alert](https://www.fda.gov/medical-devices/safety-communications/risk-false-results-curative-sars-cov-2-test-covid-19-fda-safety-communication?ref=fdaweb.com) about false result risks (mostly false negatives). At the time, the alert said that to reduce the risk of false negative results, it is important to perform the test in accordance with its authorized labeling, e.g., the [Fact Sheet for Healthcare Providers](https://www.fda.gov/media/137087/download?ref=fdaweb.com).