Cleared Special

MEDILAS H RFID LASER FIBER

K121938 · Dornier Medtech America, Inc. · General & Plastic Surgery

Aug 2012

Decision

30d

Days

Class 2

Risk

About This 510(k) Submission

K121938 is an FDA 510(k) clearance for the MEDILAS H RFID LASER FIBER, a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by Dornier Medtech America, Inc. (Kennesaw, US). The FDA issued a Cleared decision on August 1, 2012, 30 days after receiving the submission on July 2, 2012. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.

Submission Details

510(k) Number	K121938 FDA.gov
FDA Decision	Cleared SESE
Date Received	July 02, 2012
Decision Date	August 01, 2012
Days to Decision	30 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.