VeriQuick

GUDID 00004969673664

At Home Marijuana Test Kit

FOURSTAR GROUP INC.

Cannabinoid IVD, kit, enzyme immunoassay (EIA)

• Primary Device ID: 00004969673664
• 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	00004969673664 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-17
• Device Publish Date: 2021-02-09

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• 00049696737845: 11012637
• 00049696737838: 11012450S
• 00049696737739: 11012450MB
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