CyberWand USL Foot Switch

GUDID H891CWUSLFS2

CYBERSONICS INC

Foot-switch, electrical

• Primary Device ID: H891CWUSLFS2
• NIH Device Record Key: 1ed72458-6e32-4621-8cb1-35fe84169534
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CyberWand USL Foot Switch
• Version Model Number: CW-USLFS
• Company DUNS: 943561522
• Company Name: CYBERSONICS 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H891CWUSLFS2 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120303

FDA Product Code

• FFK: Lithotriptor, Electro-Hydraulic

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: 2016-05-20

On-Brand Devices [CyberWand USL Foot Switch]

• 00855279005306: CW-USLFS
• H891CWUSLFS2: CW-USLFS