Cleared Traditional

K913073 - DOBBHOFF(R) PERCUTANEOUS TRANSHEPAT BILIARY STENT

K913073 is an FDA 510(k) clearance for DOBBHOFF PERCUTANEOUS TRANSHEPAT BILIAR..., manufactured by Biosearch Medical Products, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FGE cleared through the Traditional 510(k) pathway after a 106-day FDA review.

K913073 · Biosearch Medical Products, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 1991
Decision
106d
Days
Class 2
Risk

K913073 is an FDA 510(k) clearance for the DOBBHOFF(R) PERCUTANEOUS TRANSHEPAT BILIARY STENT. Classified as Stents, Drains And Dilators For The Biliary Ducts (product code FGE), Class II - Special Controls.

Submitted by Biosearch Medical Products, Inc. (Somerville, US). The FDA issued a Cleared decision on October 25, 1991 after a review of 106 days - within the typical 510(k) review window.

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 Biosearch Medical Products, Inc. devices

FDA 510(k) Submission Details - K913073

510(k) Number K913073 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 11, 1991
Decision Date October 25, 1991
Days to Decision 106 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
25d faster than avg
Panel avg: 131d · This submission: 106d
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 400
Devices cleared under the same product code (FGE) and FDA review panel - the closest regulatory comparables to K913073.
WILTEK LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER
K914881 · Wiltek Medical, Inc. · Jan 1992
WILTEK BALLOON CHOLANGIOGRAPHY CATHETER
K914882 · Wiltek Medical, Inc. · Jan 1992
PERCUTANEOUS DILATOR WITH SHEATH
K913932 · Interventional Therapeutics Corp. · Nov 1991
2 LUMEN ENDOS RETRO CHOLANGIOPANCREA INJEC CATH
K913841 · Endovations · Oct 1991
LAPAROSCOPIC CHOLANGIOGRAPHY CATHETER WITH BALLOON
K911630 · Baxter Healthcare Corp · Sep 1991
CHOLANGIOGRAPHY CATHETER
K912122 · Wiltek Medical, Inc. · Sep 1991