Cleared Traditional

K980142 - FEATHERLITE DIODE LASER

K980142 is an FDA 510(k) clearance for FEATHERLITE DIODE LASER, manufactured by Laserlite, LLC. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K980142 · Laserlite, LLC · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Apr 1998
Decision
78d
Days
Class 2
Risk

K980142 is an FDA 510(k) clearance for the FEATHERLITE DIODE LASER. 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 Laserlite, LLC (Boston, US). The FDA issued a Cleared decision on April 3, 1998 after a review of 78 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 Laserlite, LLC devices

FDA 510(k) Submission Details - K980142

510(k) Number K980142 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 15, 1998
Decision Date April 03, 1998
Days to Decision 78 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
37d faster than avg
Panel avg: 115d · This submission: 78d
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 1883
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K980142.
DERMABLATE ER: YAG LASER SYSTEM
K980361 · Aesculap-Meditec North America · Apr 1998
LASERLITE DIODE SURGICAL LASER
K981090 · Laserlite, LLC · Apr 1998
ND: YAG ACCESSORY FOR PHOTODERM SYSTEM
K980537 · Esc Medical Systems , Ltd. · Apr 1998
MLT R694 RUBY LASER SYSTEM
K980187 · Medical Laser Technologies , Ltd. · Apr 1998
E3 MICROPROBE
K974878 · Martin Uram, MD · Mar 1998
LASERSCOPE EL LASER SYSTEM AND ACCESSORIES
K974896 · Laserscope · Mar 1998