Cleared Traditional

K905124 - MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE

K905124 is an FDA 510(k) clearance for MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE, manufactured by Red Wing Imaging, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code GCT cleared through the Traditional 510(k) pathway after a 72-day FDA review.

K905124 · Red Wing Imaging, Inc. · Gastroenterology & Urology device
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Jan 1991
Decision
72d
Days
Class 2
Risk

K905124 is an FDA 510(k) clearance for the MULTIPLE IMAGING XENON ARC AUTO LIGH SOURCE. Classified as Light Source, Endoscope, Xenon Arc (product code GCT), Class II - Special Controls.

Submitted by Red Wing Imaging, Inc. (Norwell, US). The FDA issued a Cleared decision on January 25, 1991 after a review of 72 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 Red Wing Imaging, Inc. devices

FDA 510(k) Submission Details - K905124

510(k) Number K905124 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 1990
Decision Date January 25, 1991
Days to Decision 72 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
58d faster than avg
Panel avg: 130d · This submission: 72d
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 K905124.
SYSTEM 3000 XENON VIDEOLAP LIGHT
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ENDOSCOPIC LIGHT SOURCE
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THE KEYMED HI-LIGHT 250 LIGHT SOURCE
K864801 · Keymed, Inc. · Dec 1986
PENTEX UPPER G.I. SCOPE MODEL FG-28A
K792215 · Pentax Precision Instrument Corp. · Dec 1979