FlowFlex Covid-19 Antigen Home Test, Includes 1 Tests
FlowFlex Covid-19 Antigen Home Test, Includes 1 Tests is backordered and will ship as soon as it is back in stock.
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Delivery and Shipping
Delivery and Shipping
When it comes to medical supplies, time is crucial. In most cases, orders placed on our website Monday through Friday before 4 pm Eastern Standard Time (EST) will be dispatched the same day, ensuring you receive your essential supplies without delay.
For orders placed after our business hours on Friday, or any time during the weekend (Saturday and Sunday), please note that they will be processed for shipment on the following business day, which is Monday. Your well-being is our top priority, and we're committed to delivering your critical medical supplies swiftly and efficiently.
If you have any questions or need help placing an order, don't hesitate to call us toll-free at 866-923-1544.
FlowFlex Covid-19 Antigen Home Test, Includes 1 Tests
- Flowflex Covid-19 Antigen Home Test
- DOES NOT require Serial Screening
- Nasal Swab Test
- For use with and without symptoms
- For ages 2 and up
Features / Benefits
- Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in anterior nasal swab specimens directly from individuals within 7 days of symptom onset or without symptoms or other epidemiological reasons to suspect COVID-19 infection
- Test is authorized for non-prescription home use with self-collected anterior nasal swab specimens directly from individuals aged 14 years and older or with adult-collected anterior nasal samples directly from individuals aged 2 years or older
- Excellent performance when compared to an FDA authorized molecular SARS-CoV-2 test
- Product has not been FDA cleared or approved but has been authorized by FDA under an EUA
- Product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens
- 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 soone
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