Cleared Traditional

K151714 - Disposable Endoscope Valves Set A

K151714 is an FDA 510(k) clearance for Disposable Endoscope Valves Set A, manufactured by Wilson Instruments (Shanghai) Company Limited. The device is a Class 2 Gastroenterology & Urology device with product code ODC cleared through the Traditional 510(k) pathway after a 161-day FDA review.

K151714 · Wilson Instruments (Shanghai) Company Limited · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Dec 2015
Decision
161d
Days
Class 2
Risk

K151714 is an FDA 510(k) clearance for the Disposable Endoscope Valves Set A. Classified as Endoscope Channel Accessory (product code ODC), Class II - Special Controls.

Submitted by Wilson Instruments (Shanghai) Company Limited (Shanghai, CN). The FDA issued a Cleared decision on December 3, 2015 after a review of 161 days - an extended review 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: 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 Wilson Instruments (Shanghai) Company Limited devices

FDA 510(k) Submission Details - K151714

510(k) Number K151714 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 25, 2015
Decision Date December 03, 2015
Days to Decision 161 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
31d slower than avg
Panel avg: 130d · This submission: 161d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ODC Device Classification - Class 2, Special Controls

Product Code ODC Endoscope Channel Accessory
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Give The Endoscope Channel Additional Or Improved Functionality.
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 - ODC Endoscope Channel Accessory

All 51
Devices cleared under the same product code (ODC) and FDA review panel - the closest regulatory comparables to K151714.
Endoscopic Cap, Check-Flo Adapter, Side-arm Adapter, Tuohy-Borst Adapter
K173105 · Cook Incorporated · Mar 2018
Accessory Irrigation Adapter
K162142 · Wilson-Cook Medical, Inc. · Apr 2017
SmartStart Air/Water and Suction Valves
K160403 · Endochoice, Inc. · May 2016
BioGuard Air/Water Valve, BioGuard Suction Valve
K151345 · United States Endoscopy Group, Inc. · Aug 2015
CONCENTRIC BALLOON GOOGLE
K112698 · United States Endoscopy Group, Inc. · May 2012
ETHICON ENDO SURGERY SHEATH AND ARTICULATING ACCESSORY CHANNEL - GASTROSCOPE, MODEL IN0431
K073484 · Ethicon Endo-Surgery, Inc. · Mar 2008