Cleared Traditional

K062551 - NEXUS IRRIGATION TUBING SET

K062551 is an FDA 510(k) clearance for NEXUS IRRIGATION TUBING SET, manufactured by Nexus Medical, LLC. The device is a Class 2 Gastroenterology & Urology device with product code LJH cleared through the Traditional 510(k) pathway after a 107-day FDA review.

K062551 · Nexus Medical, LLC · Gastroenterology & Urology device
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Dec 2006
Decision
107d
Days
Class 2
Risk

K062551 is an FDA 510(k) clearance for the NEXUS IRRIGATION TUBING SET. Classified as System, Irrigation, Urological (product code LJH), Class II - Special Controls.

Submitted by Nexus Medical, LLC (Lenexa, US). The FDA issued a Cleared decision on December 15, 2006 after a review of 107 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 Nexus Medical, LLC devices

FDA 510(k) Submission Details - K062551

510(k) Number K062551 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 30, 2006
Decision Date December 15, 2006
Days to Decision 107 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
23d faster than avg
Panel avg: 130d · This submission: 107d
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 10
Devices cleared under the same product code (LJH) and FDA review panel - the closest regulatory comparables to K062551.
Karl Storz UROMAT E.A.S.I.
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FLO ASSISTANT, MODEL 4-250-00
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KSEA UROPUMP
K981615 · KARL STORZ Endoscopy-America, Inc. · Jul 1998
KARL STORZ MODEL 203020 20 EQUIMAT
K971982 · KARL STORZ Endoscopy-America, Inc. · Aug 1997
MEDLINE Y-TYPE TUR/BLADDER IRRIGATION SET
K970946 · Medline Industries, Inc. · Jun 1997
TUR,ARTHROSCOPIC,CYSTOSCOPY IRRIGATION SETS
K960787 · Baxter Healthcare Corp · May 1996