Skip to content
CareStart™ COVID-19 Antigen Home Test

CareStart™ COVID-19 Antigen Home Test

by AccessBio
$34.99
$34.99 - $34.99
$34.99
$31.99
$31.99 - $31.99
$31.99
The CareStart™ COVID-19 Antigen Home Test is a rapid, lateral flow immunoassay intended for the qualitative detection of SARS-CoV-2 nucleocapsid protein antigens from individuals with or without symptoms or other epidemiological reasons to suspect a COVID-19 infection when tested twice over two or three days with at least 24 hours and not more than 48 hours between tests. This test is authorized for non-prescription home use with self-collected direct anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal swab samples from individuals aged 2 years or older.

CONTENTS 

2 CareStartTM COVID-19 Ag Home Test Devices 

2 Nasal Swabs 

2 Extraction Vial Tubes  

2 Extraction Vial Caps  

Quick Reference Instructions & Fact Sheet for Individuals 


Bullet Points
  • HOME USE TEST AUTHORIZED BY FDA UNDER AN EUA: The CareStartTM COVID-19 Antigen Home Test is authorized for non-prescription home use with self-collected direct anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal swab samples from individuals aged 2 years or older. The test can be used on individuals with or without symptoms.
  • FAST AND ACCURATE RESULTS: The test can be read 10 minutes after sample application and has 95% accuracy!
  • FREE MOBILE APP: Use the On/GoTM app with iOS or Android smartphones for free to aid in the use of the test and for rapid uploading of user test information. Access to the app is easy using the QR code available on the test box.
  • PRACTICAL SIZING AND EASY TO SHARE YOUR RESULTS: The test comes in a kit box with everything you need to perform 2 tests. Using the app, it is easy for families, schools, and workplaces to track test result data.
  • MANUFACTURED IN THE USA

 

Disclaimer
 
This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA. This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens. 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. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.