Cleared Traditional

K880592 - LASEGUIDE 600A

K880592 is an FDA 510(k) clearance for LASEGUIDE 600A, manufactured by Laser Peripherals, LLC. The device is a Class 2 Anesthesiology device with product code LLO cleared through the Traditional 510(k) pathway after a 74-day FDA review.

K880592 · Laser Peripherals, LLC · Anesthesiology device
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Apr 1988
Decision
74d
Days
Class 2
Risk

K880592 is an FDA 510(k) clearance for the LASEGUIDE 600A, 600B, 400A, 400B FOR PULMONARY USE. Classified as Laser, Neodymium:yag, Pulmonary Surgery (product code LLO), Class II - Special Controls.

Submitted by Laser Peripherals, LLC (Hingham, US). The FDA issued a Cleared decision on April 25, 1988 after a review of 74 days - a notably fast clearance cycle.

This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 874.4500 - the FDA anesthesiology and respiratory 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 Laser Peripherals, LLC devices

FDA 510(k) Submission Details - K880592

510(k) Number K880592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 11, 1988
Decision Date April 25, 1988
Days to Decision 74 days
Submission Type Traditional
Review Panel Anesthesiology (AN)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
66d faster than avg
Panel avg: 140d · This submission: 74d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LLO Device Classification - Class 2, Special Controls

Product Code LLO Laser, Neodymium:yag, Pulmonary Surgery
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 874.4500
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 Anesthesiology devices follow this clearance model.

Regulatory Peers - LLO Laser, Neodymium:yag, Pulmonary Surgery

All 10
Devices cleared under the same product code (LLO) and FDA review panel - the closest regulatory comparables to K880592.
SLT CLMD CONTACT LASER
K884815 · Surgical Laser Technologies, Inc. · Dec 1988
SURGILASE YAG 100 FOR GYNECOLOGY USE
K881499 · Surgilase, Inc. · Apr 1988
MODEL 4900 ND:YAG LASER FOR PULMONARY OBSTRUCTIONS
K880170 · Cooper Lasersonics, Inc. · Mar 1988
OPTILASE YAG MODEL 1000 SURG LASER SYS/PULMON APPL
K870505 · Trimedyne, Inc. · Aug 1987
6000 ND:YAG LASER FOR BENIGN/MALIGNANT OBSTRUCTION
K862698 · Cooper Lasersonics, Inc. · Aug 1986
LASER BRONCHOSCOPE SYSTEM
K861921 · Pilling Co. · Jun 1986