VeriQuick

GUDID 00049696726030

VeriQuick Marijuana Drug Test for Family Dollar

FOURSTAR GROUP INC.

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• Primary Device ID: 00049696726030
• NIH Device Record Key: abbdc0ee-9476-4c28-b9a2-b1ad9a3f159b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriQuick
• Version Model Number: 4969672603
• Company DUNS: 656091279
• Company Name: FOURSTAR GROUP INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does n
• 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	00049696726030 [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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-04-27

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