Cleared Traditional

K894592 - LAMANO DIRECTORS

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

K894592 · Marlo Surgical Technology · Gastroenterology & Urology device
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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

FDA 510(k) Submission Details - K894592

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
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
85d faster than avg
Panel avg: 131d · This submission: 46d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCM Device Classification - Class 2, Special Controls

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 12
Devices cleared under the same product code (GCM) and FDA review panel - the closest regulatory comparables to K894592.
KARL STORZ PLASTIC SURGERY ACCESSORIES
K945889 · KARL STORZ Endoscopy-America, Inc. · Mar 1995
THORACOSCOPE/LAPAROSCOPE
K931954 · Surgical Technologies, Inc. · Nov 1993
PRESSURE TURING AND ACCESSORIES
K925918 · Applied Medical Resources · Feb 1993
RIGID ENDOSCOPE
K853514 · American Edwards Laboratories · Oct 1985
RIGID FIBEROPITC ENDOSCOPE
K844769 · Microvasive · Jan 1985