QuickVue SARS Antigen Test
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QuickVue SARS Antigen
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The QuickVue SARS Antigen Test



Test type: Lateral flow immunoassay
Specimen type:
 Nasal (NS) swab specimen
Turnaround time:
 10-15 minutes
FDA status: 
Emergency Use Authorization (EUA) Granted
CLIA complexity:
Waived, Moderate, or High


  • *This product has not been FDA cleared or approved; but has been authorized by FDA under an EUA for use by authorized laboratories;
  • This product has been authorized only for the detection of proteins from SARS- CoV-2, not for any other viruses or pathogens; and,
  • 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.

Features :

  • Hygienic Product : Not Specified
  • Allergy : Not Specified
  • UPC:Not Specified
  • GTIN/ITF Barcode : Not Specified
  • Units of Measure : Not Specified
  • Overall Product Length : Not Specified in
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  • Weight Capacity : Not Specified lbs
  • Actual Product Weight : 0.80
  • Product Assembly : Not Specified
  • Product Installation : Not Specified
  • Country of Origin : Not Specified
  • Case QTY : Not Specified/case
  • Case Weight : Not Specified
  • Ships Via Freight : No
  • Proposition 65 Warning : Not Specified