Profound, SubQ Single- Use Cartridge, Packaged

GUDID 00817495024370

Profound, SubQ Single- Use Cartridge, Packaged

Candela Corporation

Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system Multi-modality skin surface treatment system

• Primary Device ID: 00817495024370
• NIH Device Record Key: 652138ed-ec5d-42ef-8f02-9858373049ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Profound, SubQ Single- Use Cartridge, Packaged
• Version Model Number: AS87913
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	00817495024370 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161043

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-08
• Device Publish Date: 2024-02-29

Devices Manufactured by Candela Corporation

• 00817495024370 - Profound, SubQ Single- Use Cartridge, Packaged: 2024-03-08Profound, SubQ Single- Use Cartridge, Packaged
• 00817495024370 - Profound, SubQ Single- Use Cartridge, Packaged: 2024-03-08 Profound, SubQ Single- Use Cartridge, Packaged
• 00817495024387 - Profound, Dermal Single- Use Cartridge, Packaged: 2024-03-08 Profound, Dermal Single- Use Cartridge, Packaged
• 00817495023854 - GMPP Modified LSDS (HRDS) Options Kit for DCD: 2024-02-28 GMPP Modified LSDS (HRDS) Options Kit for DCD
• 00817495023915 - GMPP Modified LSDS (HRDS) Options Kit for ACC: 2024-02-28 GMPP Modified LSDS (HRDS) Options Kit for ACC
• 00817495025032 - HRDS Handpiece DCD Cooled: 2024-02-28 HRDS Handpiece DCD Cooled
• 00817495025049 - HRDS Handpiece Air Cooled: 2024-02-28 HRDS Handpiece Air Cooled
• 00817495024882 - Canister HFO-R1234 ZE / 950g, ALUM (US): 2024-02-12 Canister HFO-R1234 ZE / 950g, ALUM (US)
• 00817495024905 - Canister HFO-R1234 ZE / 950g, ALUM (Japan): 2024-02-12 Canister HFO-R1234 ZE / 950g, ALUM (Japan)