FSE PF1 6-18MM Delivery System W/DCD Assembly 7122-57-3956

GUDID 08174950202547

Delivery System Assembly

CANDELA CORPORATION

Dermatological solid-state laser system

• Primary Device ID: 08174950202547
• NIH Device Record Key: 20748285-0aaa-43de-a6d5-d5767190276b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FSE PF1 6-18MM Delivery System W/DCD Assembly
• Version Model Number: 7122-57-3956
• Catalog Number: 7122-57-3956
• Company DUNS: 053468385
• Company Name: CANDELA CORPORATION
• 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	08174950202547 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140732

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-06
• Device Publish Date: 2016-10-03

On-Brand Devices [FSE PF1 6-18MM Delivery System W/DCD Assembly]

• 08174950202547: Delivery System Assembly
• 00817495022543: Delivery System Assembly