Vectus

Basic Information

• Brand Name: Vectus
• Primary DI: 00841494100124
• Version / Model: 105-3500-000
• Company Name: Cynosure, LLC
• Labeler DUNS: 780318028
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2016-09-24
• Public Version: 5
• Public Version Date: 2023-01-11
• Public Version Status: Update
• Public Device Record Key: e2a127c1-f0b2-47fb-90ed-776fb71e687d

Device Description

Vectus Laser Assembly

Device Characteristics

• Single Use: No
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: Yes
• Has Lot/Batch Number: No
• Has Manufacturing Date: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
GEX	Powered laser surgical instrument	General, Plastic Surgery	878.4810	2

GMDN Terms

Code	Name	Definition	Implantable	Status
58525	Dermatological Raman spectroscopy system	A mains electricity (AC-powered) device assembly intended to be used by a healthcare professional to non-invasively evaluate a skin lesion clinically suspicious for carcinoma (e.g., melanoma, squamous cell) and precursors, before making a decision to biopsy, that operates based on inelastic (Raman) scattering of monochromatic light to measure molecular vibrations and identify pathology associated tissue molecules (e.g., proteins, lipids). It is an optical system applied to the skin surface typically consisting of a hardware unit (e.g., diode laser, fibreoptic system, Raman probe, spectrograph, image sensor chip, detector, computer), software, and a connected probe used to scan the lesion.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00841494100124	GS1

Premarket Submissions

Submission Number	Supplement Number
K120622	000