Cleared Traditional

K894592 - LAMANO DIRECTORS

K894592 is the FDA 510(k) clearance for LAMANO DIRECTORS by Marlo Surgical Technology. It is a Class 2 Gastroenterology & Urology device (product code GCM) cleared through the Traditional 510(k) pathway after a 46-day FDA review.

K894592 · Marlo Surgical Technology · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Sep 1989
Decision
46d
Days
Class 2
Risk

K894592 is an FDA 510(k) clearance for the LAMANO DIRECTORS. Classified as Endoscope, Rigid (product code GCM), Class II - Special Controls.

Submitted by Marlo Surgical Technology (Willoughby, US). The FDA issued a Cleared decision on September 8, 1989 after a review of 46 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - the FDA gastroenterology and urology 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 Marlo Surgical Technology devices

Submission Details

510(k) Number K894592 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 24, 1989
Decision Date September 08, 1989
Days to Decision 46 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
84d faster than avg
Panel avg: 130d · This submission: 46d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GCM Endoscope, Rigid
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - GCM Endoscope, Rigid

All 8
Devices cleared under the same product code (GCM) and FDA review panel - the closest regulatory comparables to K894592.
ENDOSCOPY SYSTEM FOR FACIAL PLASTIC SURGERY
K935235 · Smith & Nephew Richards, Inc. · Mar 1995
KARL STORZ PLASTIC SURGERY ACCESSORIES
K945889 · KARL STORZ Endoscopy-America, Inc. · Mar 1995
PRESSURE TURING AND ACCESSORIES
K925918 · Applied Medical Resources · Feb 1993
RIGID ENDOSCOPE
K853514 · American Edwards Laboratories · Oct 1985