Cleared Traditional

K910716 - MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE

K910716 is an FDA 510(k) clearance for MODEL 2144.00 COMBINATION ENDO-SURGICAL..., manufactured by Richard Wolf Medical Instruments Corp.. The device is a Class 2 Gastroenterology & Urology device with product code FCX cleared through the Traditional 510(k) pathway after a 55-day FDA review.

K910716 · Richard Wolf Medical Instruments Corp. · Gastroenterology & Urology device
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Apr 1991
Decision
55d
Days
Class 2
Risk

K910716 is an FDA 510(k) clearance for the MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE. Classified as Insufflator, Automatic Carbon-dioxide For Endoscope (product code FCX), Class II - Special Controls.

Submitted by Richard Wolf Medical Instruments Corp. (Rosemont, US). The FDA issued a Cleared decision on April 16, 1991 after a review of 55 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.

FDA 510(k) Submission Details - K910716

510(k) Number K910716 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 20, 1991
Decision Date April 16, 1991
Days to Decision 55 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
76d faster than avg
Panel avg: 131d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FCX Device Classification - Class 2, Special Controls

Product Code FCX Insufflator, Automatic Carbon-dioxide For Endoscope
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 - FCX Insufflator, Automatic Carbon-dioxide For Endoscope

All 24
Devices cleared under the same product code (FCX) and FDA review panel - the closest regulatory comparables to K910716.
E-Z-FLATE
K930581 · E-Z-Em, Inc. · Jul 1994
INSUFFLATION TUBING SET, PHX500-082
K935059 · Phx Technologies Corp. · Dec 1993
HIFLO FILTERED INSUFFLATION TUBING
K930508 · W. J. Medical Instruments, Inc. · Jun 1993
OLYMPUS-KEYMED ENDOSCOPIC CO2 REGULATOR, MODEL ECR
K881004 · Keymed, Inc. · May 1988
ENDOSCOPIC MANUAL AIR INSUFFLATOR
K844689 · Jayco Pharmaceuticals · Jan 1985
K910716 · MODEL 2144.00 COMBINATION ENDO-SURGICAL DEVICE
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