Cleared Traditional

K972872 - DERMA K LASER SYSTEM

K972872 is an FDA 510(k) clearance for DERMA K LASER SYSTEM, manufactured by Esc Medical Systems , Ltd.. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K972872 · Esc Medical Systems , Ltd. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1997
Decision
85d
Days
Class 2
Risk

K972872 is an FDA 510(k) clearance for the DERMA K LASER SYSTEM. Classified as Powered Laser Surgical Instrument within the GEX classification (a category for powered laser surgical instruments across multiple specialties), Class II - Special Controls.

Submitted by Esc Medical Systems , Ltd. (Yokneam, IL). The FDA issued a Cleared decision on October 28, 1997 after a review of 85 days - a notably fast clearance cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4810 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Esc Medical Systems , Ltd. devices

FDA 510(k) Submission Details - K972872

510(k) Number K972872 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 04, 1997
Decision Date October 28, 1997
Days to Decision 85 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
30d faster than avg
Panel avg: 115d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GEX Device Classification - Class 2, Special Controls

Product Code GEX Powered Laser Surgical Instrument
Device Class Class 2 - 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.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GEX Powered Laser Surgical Instrument

All 1881
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K972872.
CYNOSURE PHOTOGENICA ER LASER
K973498 · Cynosure, Inc. · Nov 1997
PROTEGE ER:YAG LASER SYSTEM AND ACCESSORIES
K971912 · Xintec Corporation · Nov 1997
C4
K970143 · Clinicon Corp. · Oct 1997
LASETTE
K973431 · Cell Robotics, Inc. · Oct 1997
DERMASCAN SURGICAL LASER SCANNER
K972028 · Esc Medical Systems , Ltd. · Oct 1997
NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER
K972765 · American Laser Medical · Oct 1997