VeriQuick

GUDID 00049696736664

At Home Marijuana Test Kit

FOURSTAR GROUP INC.

Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA) Cannabinoid/cannabinoid metabolite IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00049696736664
• NIH Device Record Key: ab5ebfea-fa93-4de8-9d71-31ddf70d5382
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriQuick
• Version Model Number: 11012637
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00049696736664 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140546

FDA Product Code

• LDJ: Enzyme Immunoassay, Cannabinoids

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-02-24
• Device Publish Date: 2021-02-09

On-Brand Devices [VeriQuick]

• 00049696726054: VeriQuick Ovulation Predictor Test for Family Dollar
• 00049696726047: VeriQuick Pregnancy Test for Family Dollar
• 00049696726030: VeriQuick Marijuana Drug Test for Family Dollar
• 00049696609531: 171444
• 00049696736671: Ovulation Predictor
• 00049696736657: Pregnancy Test
• 00004969673664: At Home Marijuana Test Kit
• 00049696736664: At Home Marijuana Test Kit
• 00049696737845: 11012637
• 00049696737838: 11012450S
• 00049696737739: 11012450MB
• 00049696128032: PREGNANCY TEST 2CT
• 00049696739344: MULTI-DRUG URINE TEST DIP CARD
• 00049696708319: AT HOME MULTI-DRUG TEST