Live View Panel Pro Version 2.0

GUDID 00817111021264

Live View Panel Pro Version 2.0

Neurotronics, LLC

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• Primary Device ID: 00817111021264
• NIH Device Record Key: 7f5dbe98-74bd-4ee7-afc4-b1814a5409dd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Live View Panel Pro Version 2.0
• Version Model Number: 2.0
• Company DUNS: 036405363
• Company Name: Neurotronics, LLC
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817111021264 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131415

FDA Product Code

• GWQ: Full-Montage Standard Electroencephalograph

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: 2024-05-17
• Device Publish Date: 2024-05-09

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