Cleared Traditional

K971193 - LASEAWAY LONG PULSE AND Q-SWITCHED RUBY LASER SYSTEM

K971193 is an FDA 510(k) clearance for LASEAWAY LONG PULSE AND Q-SWITCHED RUBY..., manufactured by Polytec Pi, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K971193 · Polytec Pi, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1997
Decision
84d
Days
Class 2
Risk

K971193 is an FDA 510(k) clearance for the LASEAWAY LONG PULSE AND Q-SWITCHED RUBY 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 Polytec Pi, Inc. (Great Neck,, US). The FDA issued a Cleared decision on June 24, 1997 after a review of 84 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 Polytec Pi, Inc. devices

FDA 510(k) Submission Details - K971193

510(k) Number K971193 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 01, 1997
Decision Date June 24, 1997
Days to Decision 84 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
31d faster than avg
Panel avg: 115d · This submission: 84d
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 K971193.
CELL ROBOTICS ER: YAG SURGICAL LASER
K970461 · Cell Robotics, Inc. · Jul 1997
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K971404 · Schwartz Electro-Optics, Inc. · Jul 1997
LASERSCOPE MICROBEAM IV MICROMANIPULATOR
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ORION SERIES SURGICAL LASER SYSTEM (Q-SWITCHED ND:YAG CONFIGURATION)
K964818 · Laserscope · Jun 1997
SOFTSCAN
K971024 · Sahar Technologies, Inc. · Jun 1997
DENTICA PULSED ND: YAG LASER SYSTEMS AND ACCESSORIES
K971065 · Xintec Corporation · Jun 1997