Cleared Traditional

K913841 - 2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATH

K913841 is an FDA 510(k) clearance for 2 LUMEN ENDOS RETRO CHOLANGIOPANCREA IN..., manufactured by Endovations. The device is a Class 2 Gastroenterology & Urology device with product code FGE cleared through the Traditional 510(k) pathway after a 43-day FDA review.

K913841 · Endovations · Gastroenterology & Urology device
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Oct 1991
Decision
43d
Days
Class 2
Risk

K913841 is an FDA 510(k) clearance for the 2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATH. Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Endovations (Mechanicsburg, US). The FDA issued a Cleared decision on October 8, 1991 after a review of 43 days - a notably fast clearance 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: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Endovations devices

FDA 510(k) Submission Details - K913841

510(k) Number K913841 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 26, 1991
Decision Date October 08, 1991
Days to Decision 43 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
88d faster than avg
Panel avg: 131d · This submission: 43d
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 404
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K913841.
WILTEK BALLOON CHOLANGIOGRAPHY CATHETER
K914882 · Wiltek Medical, Inc. · Jan 1992
PERCUTANEOUS DILATOR WITH SHEATH
K913932 · Interventional Therapeutics Corp. · Nov 1991
DOBBHOFF(R) PERCUTANEOUS TRANSHEPAT BILIARY STENT
K913073 · Biosearch Medical Products, Inc. · Oct 1991
LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER WITH BALLOON
K911630 · Baxter Healthcare Corp · Sep 1991
CHOLANGIOGRAPHY CATHETER
K912122 · Wiltek Medical, Inc. · Sep 1991
WILTEK STANDARD CHOLANGIOGRAPHY CATHETER
K912288 · Wiltek Medical, Inc. · Sep 1991