Cleared Traditional

K923210 - SYSTEM 3000 XENON VIDEOLAP LIGHT

K923210 is an FDA 510(k) clearance for SYSTEM 3000 XENON VIDEOLAP LIGHT, manufactured by Cabot Medical Corp.. The device is a Class 2 Gastroenterology & Urology device with product code GCT cleared through the Traditional 510(k) pathway after a 96-day FDA review.

K923210 · Cabot Medical Corp. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1992
Decision
96d
Days
Class 2
Risk

K923210 is an FDA 510(k) clearance for the SYSTEM 3000 XENON VIDEOLAP LIGHT. Classified as Light Source, Endoscope, Xenon Arc (product code GCT), Class II - Special Controls.

Submitted by Cabot Medical Corp. (Langhorne, US). The FDA issued a Cleared decision on October 5, 1992 after a review of 96 days - within the typical 510(k) review window.

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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Cabot Medical Corp. devices

FDA 510(k) Submission Details - K923210

510(k) Number K923210 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 01, 1992
Decision Date October 05, 1992
Days to Decision 96 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
34d faster than avg
Panel avg: 130d · This submission: 96d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GCT Device Classification - Class 2, Special Controls

Product Code GCT Light Source, Endoscope, Xenon Arc
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 - GCT Light Source, Endoscope, Xenon Arc

All 21
Devices cleared under the same product code (GCT) and FDA review panel - the closest regulatory comparables to K923210.
ZEISS SUPERLUX HIGH-INTENSITY LIGHT SOURCES
K936198 · Carl Zeiss, Inc. · Apr 1994
XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300
K924897 · Medical Devices, Inc. · Jul 1993
PENTAX XENON LIGHT SOURCE
K921315 · Pentax Precision Instrument Corp. · Jun 1993
MARLOW VERRES NEEDLES
K913586 · Marlo Surgical Technology · Oct 1991
ENDOSCOPIC LIGHT SOURCE
K911492 · United States Endoscopy Group, Inc. · Aug 1991
THE KEYMED HI-LIGHT 250 LIGHT SOURCE
K864801 · Keymed, Inc. · Dec 1986