Cleared Traditional

K954713 - DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION)

K954713 is an FDA 510(k) clearance for DURAL-LUMEN INTRA VASCULAR BALLOON CATH..., manufactured by Ideas For Medicine, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FGE cleared through the Traditional 510(k) pathway after a 288-day FDA review.

K954713 · Ideas For Medicine, Inc. · Gastroenterology & Urology device
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Optimized for regulatory review, auditing and printing
Jul 1996
Decision
288d
Days
Class 2
Risk

K954713 is an FDA 510(k) clearance for the DURAL-LUMEN INTRA VASCULAR BALLOON CATHETER (MODIFICATION). Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Ideas For Medicine, Inc. (Clearwater, US). The FDA issued a Cleared decision on July 24, 1996 after a review of 288 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 Ideas For Medicine, Inc. devices

FDA 510(k) Submission Details - K954713

510(k) Number K954713 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 10, 1995
Decision Date July 24, 1996
Days to Decision 288 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
157d slower than avg
Panel avg: 131d · This submission: 288d
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 409
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K954713.
ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER
K963397 · Boston Scientific Corp · Nov 1996
NAVARRE PERCUTANEOUS BILIARY DRAINAGE
K955110 · Navarre Biomedical , Ltd. · 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
LMI BILIARY CATHETER
K955126 · Lucas Medical, Inc. · May 1996
WALLSTENT TRANSHEPATIC BILIARY ENDOPROSTHESIS/WALLSTENT ENDOSCOPIC BILIARY ENDOPROSTHESIS
K961262 · Boston Scientific Scimed, Inc. · May 1996