3 COVID-19 Tests & Cue Reader
$349
Cue+ Member Price$294.20
Cue's COVID-19 test is an FDA-authorized* at-home test to detect SARS-CoV-2, the virus that causes COVID-19. Cue’s test matched lab results with 97.8% accuracy in an independent study by Mayo Clinic. Results are delivered to your mobile smart device in 20 minutes.
If you test positive for COVID-19 with your Cue test, you can get Cue Care® through the Cue Health App at no additional cost, which includes a telehealth consult and same-day medication delivery, if prescribed (cost of medication not included).
• Results in 20 minutes
• Must be used with a Cue Reader (included)
• HSA/FSA eligible
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Tests
Telehealth
About
3 COVID-19 Tests & Cue Reader
Better care starts
with Cue
How It Works
with Cue
Access fast, convenient care and discreet home delivery today. Get started in 4 easy steps.
Insert your Cartridge into the Reader
Use the Wand to collect a sample from the lower part of each nostril
Insert the Wand into the Cartridge
Receive results in 20 minutes via the Cue Health App
Cue customers say it best
It's amazing how easy and convenient Cue is to use. And getting highly accurate results in just 20 minutes is a game changer for me.
Luis V.
Los Angeles, CA
I carry my Cue everywhere I travel. Its ability to get a near-instant, supervised digital test result on my phone has been a lifesaver to comply with the constantly changing location-specific testing requirements.
Aaron W.
New York, NY
Since I discovered Cue COVID-19 tests, traveling has been way easier! Cue made my digital nomad life even better and more secure! I love how quick the results come in.
Isabel Q.
San Francisco, CA
Carrying Cue in my bag while traveling has allowed me to get lab-quality results abroad and within 20 minutes, removing the hassle of finding testing sites compliant with the regulatory administrations internationally.
Alberto P.
Chicago, IL
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*Cue COVID-19 Test for Home and Over The Counter (OTC) Use: The Cue COVID-19 Test for Home and Over The Counter (OTC) Use has not been FDA cleared or approved, but it has been authorized by the FDA under an Emergency Use Authorization (EUA). This product has been authorized only for the detection of nucleic acid 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 in vitro diagnostics 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.
Resources
¹ https://covid.cdc.gov/covid-data-tracker/#datatracker-home
² https://covid19.who.int/#:~:text=Globally%2C%20as%20of%204%3A24pm,vaccine%20doses%20have%20been%20administered.
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