Emergency Use Authorization for Flowflex Plus COVID-19 & Flu A/B Combo Test

Emergency Use Authorization for Flowflex Plus COVID-19 and Flu A/B Combo Test

Emergency Use Authorization for Flowflex Plus COVID-19 & Flu A/B Combo Test

The Acon Laboratories Flowflex Plus COVID-19 and Flu A/B Home Test has received Emergency Use Authorization (EUA) from the FDA.

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The Acon Laboratories Flowflex Plus COVID-19 and Flu A/B Home Test has received Emergency Use Authorization (EUA) from the FDA. This advanced diagnostic tool is designed to detect both SARS-CoV-2, the virus responsible for COVID-19, as well as influenza A and B viruses, using a single sample.

This dual-detection capability addresses a critical need, especially as flu season approaches and the COVID-19 pandemic continues to impact communities worldwide. By allowing for the simultaneous detection of both COVID-19 and influenza, the Flowflex Plus COVID-19 and Flu A/B Home Test plays an important role in differentiating between these illnesses, which present with similar symptoms but require potentially different response and treatments.

The Flowflex Plus COVID-19 and Flu A/B Antigen Home Test is designed to offer fast and accurate results within 15 minutes and can be performed at home, making it convenient for widespread use.

The ease of use and rapid results make the Flowflex Plus Combo Test ideal for workplace, point-of-care, and home settings.

DrugTestKitUSA remains committed to delivering cutting-edge diagnostic tools that meet the evolving challenges of the healthcare industry. The introduction of the Flowflex Plus COVID-19 and Flu A/B Home Test underscores this commitment by providing a reliable, easy-to-use solution for detecting both COVID-19 and influenza,  empowers the consumer to participate in their healthcare.

For more information about the Flowflex Plus Combo Test and DrugTestKitUSA’s comprehensive range of diagnostic products, please visit DrugtestkitUSA.com

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