CS6101 Interferential Kit

GUDID 00860009424722

CS6101-2-K01 Interferential Kit

Control Solutions LLC

Physical therapy ultrasound/neuromuscular stimulation system

• Primary Device ID: 00860009424722
• NIH Device Record Key: 36fef5f8-763f-4eff-97da-206086b10eab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CS6101 Interferential Kit
• Version Model Number: CS6101-2-K01 Interferential Kit
• Company DUNS: 829053201
• Company Name: Control Solutions 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860009424722 [Primary]

FDA Product Code

• LIH: Interferential Current Therapy

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: 2023-03-28
• Device Publish Date: 2023-03-20

On-Brand Devices [CS6101 Interferential Kit]

• 00860009424722: CS6101-2-K01 Interferential Kit
• 00860009424715: CS6101-1-K01 Interferential Stimulator Kit: Contains Stimulator, lead set, one (1) set of electr