Cleared Traditional

K023808 - IRRIGATION SETS

K023808 is an FDA 510(k) clearance for IRRIGATION SETS, manufactured by International Medsurg Connection. The device is a Class 2 Gastroenterology & Urology device with product code LJH cleared through the Traditional 510(k) pathway after a 116-day FDA review.

K023808 · International Medsurg Connection · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2003
Decision
116d
Days
Class 2
Risk

K023808 is an FDA 510(k) clearance for the IRRIGATION SETS. Classified as System, Irrigation, Urological (product code LJH), Class II - Special Controls.

Submitted by International Medsurg Connection (Grayslake, US). The FDA issued a Cleared decision on March 10, 2003 after a review of 116 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5130 - 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 International Medsurg Connection devices

FDA 510(k) Submission Details - K023808

510(k) Number K023808 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 14, 2002
Decision Date March 10, 2003
Days to Decision 116 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
15d faster than avg
Panel avg: 131d · This submission: 116d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

LJH Device Classification - Class 2, Special Controls

Product Code LJH System, Irrigation, Urological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5130
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 - LJH System, Irrigation, Urological

All 18
Devices cleared under the same product code (LJH) and FDA review panel - the closest regulatory comparables to K023808.
SPYGLASS IRRIGATION SYSTEM
K063700 · Medical Scientific, Inc. · Feb 2007
NEXUS IRRIGATION TUBING SET
K062551 · Nexus Medical, LLC · Dec 2006
URO PRO
K042457 · W.O.M. World of Medicine AG · Oct 2004
FLO ASSISTANT, MODEL 4-250-00
K001325 · Northgate Technologies, Inc. · Aug 2000
MTP UROPUMP DISPOSABLE TUBING SET
K990909 · Mtp Medical Technical Promotion GmbH · Jun 1999
KSEA UROPUMP
K981615 · KARL STORZ Endoscopy-America, Inc. · Jul 1998