Cleared Special

VenaCure EVLT NeverTouch Procedure Kits; VenaCure EVLT NeverTouch Direct Procedure Kits

K231945 · AngioDynamics, Inc. · General & Plastic Surgery

Jul 2023

Decision

20d

Days

Class 2

Risk

About This 510(k) Submission

K231945 is an FDA 510(k) clearance for the VenaCure EVLT NeverTouch Procedure Kits; VenaCure EVLT NeverTouch Direct Procedure Kits, a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by AngioDynamics, Inc. (Queensbury, US). The FDA issued a Cleared decision on July 20, 2023, 20 days after receiving the submission on June 30, 2023. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.

Submission Details

510(k) Number	K231945 FDA.gov
FDA Decision	Cleared SESE
Date Received	June 30, 2023
Decision Date	July 20, 2023
Days to Decision	20 days
Submission Type	Special
Review Panel	General & Plastic Surgery (SU)
Summary	Summary PDF

Device Classification

Product Code	GEX — Powered Laser Surgical Instrument
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 878.4810
Definition	A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light.