Kit, PicoWay 532 HE Resolve HP

GUDID 08174950202905

Handpiece Kit

CANDELA CORPORATION

Laser skin surface treatment system applicator

• Primary Device ID: 08174950202905
• NIH Device Record Key: 7d9984cb-7867-477d-8e00-a13d252ffb88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Kit, PicoWay 532 HE Resolve HP
• Version Model Number: 7123-00-0593
• 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: true
• 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

Customer Support Contacts

• Phone: 800-733-8550
• Email: customer.service@candelamedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	08174950202905 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K191685

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2019-12-20
• Device Publish Date: 2019-12-12

On-Brand Devices [Kit, PicoWay 532 HE Resolve HP]

• 08174950202905: Handpiece Kit
• 00817495022901: Handpiece Kit