Cleared Traditional

K920553 - MYRIADLASE SIDEFIRE-TIPPED OPTICAL FIBER

K920553 is an FDA 510(k) clearance for MYRIADLASE SIDEFIRE-TIPPED OPTICAL FIBER, manufactured by Myriad Lase, Inc.. The device is a Class 2 General & Plastic Surgery device with product code GEX cleared through the Traditional 510(k) pathway after a 49-day FDA review.

K920553 · Myriad Lase, Inc. · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1992
Decision
49d
Days
Class 2
Risk

K920553 is an FDA 510(k) clearance for the MYRIADLASE SIDEFIRE-TIPPED OPTICAL FIBER. 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 Myriad Lase, Inc. (Forest Hill, US). The FDA issued a Cleared decision on March 26, 1992 after a review of 49 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 Myriad Lase, Inc. devices

FDA 510(k) Submission Details - K920553

510(k) Number K920553 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 06, 1992
Decision Date March 26, 1992
Days to Decision 49 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 115d · This submission: 49d
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 1880
Devices cleared under the same product code (GEX) and FDA review panel - the closest regulatory comparables to K920553.
LATERALASE
K920625 · Trimedyne, Inc. · Apr 1992
SIDE FIRING FIBERS
K920632 · Trimedyne, Inc. · Apr 1992
CO2 LASER AND WAVEGUIDE DELIVERY SYSTEMS FOR THOR.
K915583 · Heraeus Lasersonics, Inc. · Mar 1992
ZEISS MULTIYAG LASER
K915840 · Carl Zeiss, Inc. · Mar 1992
OPTICA 25 ND:YAG DENTAL LASER SYSTEM
K913839 · Xintec Corporation · Mar 1992
ADL 400 ND
K920106 · Sunrise Technologies, Inc. · Mar 1992