Cleared Traditional

K955126 - LMI BILIARY CATHETER

K955126 is an FDA 510(k) clearance for LMI BILIARY CATHETER, manufactured by Lucas Medical, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FGE cleared through the Traditional 510(k) pathway after a 183-day FDA review.

K955126 · Lucas Medical, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 1996
Decision
183d
Days
Class 2
Risk

K955126 is an FDA 510(k) clearance for the LMI BILIARY CATHETER. Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Lucas Medical, Inc. (Anaheim, US). The FDA issued a Cleared decision on May 10, 1996 after a review of 183 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5010 - 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 Lucas Medical, Inc. devices

FDA 510(k) Submission Details - K955126

510(k) Number K955126 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 09, 1995
Decision Date May 10, 1996
Days to Decision 183 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
53d slower than avg
Panel avg: 130d · This submission: 183d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FGE Device Classification - Class 2, Special Controls

Product Code FGE Stents, Drains And Dilators For The Biliary Ducts
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5010
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 - FGE Stents, Drains And Dilators For The Biliary Ducts

All 314
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K955126.
ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER
K963397 · Boston Scientific Corp · Nov 1996
OLYMPUS B-5/B-7 SERIESBALLOON CATHETER
K962925 · Olympus America, Inc. · Oct 1996
MANAN INTRODUCER SHEALTH/NEEDLE
K961216 · Manan Medical Products, Inc. · May 1996
WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS/WALLSTENT ENDOSCOPIC BILIARY ENDOPROSTHESIS
K961262 · Boston Scientific Scimed, Inc. · May 1996
CORDIS BILIARY STENT
K955728 · Cordis Corp. · May 1996
MANAN BILIARY DRAINAGE CATHETER
K954043 · Manan Medical Products, Inc. · Mar 1996