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Flowflex COVID-19 Antigen Home Test kit, 1 Pack, 1 Tests Total. FDA EUA Authorized OTC at-Home Self-Test, Non-invasive Nasal Swab, Easy to Use and No Discomfort, Results in 15 Minutes
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Flowflex COVID-19 Antigen Home Test kit, 1 Pack, 1 Features
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Expiration Date Extension: On March 15, 2023, the FDA granted the Flowflex COVID-19 Antigen Home Test another 3-month shelf-life extension, which extended the shelf-life of the product from 12 months to 24 months. Refer to the FDA website for the extended expiration dates.
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FDA EUA Authorized COVID-19 Home Test – This test is authorized for home use without the need for a prescription or sending to a lab.
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Detects Active COVID-19 Infection - This test detects multiple COVID-19 variants including the Omicron and Delta variants.
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Safe to Test Adults and Children – The test is recommended for self-collection by individuals aged 14 years and older and with adult-collection by individuals aged 2 years or older.
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Easy to Use – All the components of the nasal swab test are included inside the box with step-by-step Instructions for Use in English and Spanish. No Symptoms Needed – This test is intended to test individuals with or without COVID-19 symptoms. Quick Results – This test is quick and simple. The result is read in 15 minutes
About Flowflex COVID-19 Antigen Home Test Kit, 1 Pack, 1
A rapid test for the detection of SARS-CoV-2 antigens in anterior nasal specimens directly from individuals within 7 days of symptom onset or without symptoms or other epidemiological reasons to suspect COVID-19 infection. This product has not been FDA cleared or approved; but has been authorized by FDA under an Emergency Use Authorization. This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens. The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb-3(b)(1), unless the declaration is terminated, or authorization is revoked sooner.
