KENNIE’S PHARMACY
COVID-19 Testing

ID NOW^™ Rapid Molecular Testing Instrument

How it works.

You or the pharmacist will take a nasal sample with a swab. The analyzer then examines the sample looking to see if any bacterial or viral material is present in the sample. The test then confirms you are negative or positive for the infection. Positive results should be confirmed with your care provider.

The ID NOW COVID-19 EUA has not been FDA cleared or approved. It has been authorized by the FDA under an emergency use authorization for use by authorized laboratories and patient care settings. The test has been authorized only for the detection of nucleic acid from SARS-CoV-2, not for any other viruses or pathogens, and is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner. © 2021 Abbott. All rights reserved. All trademarks referenced are trademarks of either the Abbott group of companies or their respective owners. COL-03258-02 05/2021