Cleared Traditional

K865085 - KAMINSKY COMBINATION STENT & INJECTION CATHETER

K865085 is an FDA 510(k) clearance for KAMINSKY COMBINATION STENT & INJECTION ..., manufactured by Van-Tec, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code FAD cleared through the Traditional 510(k) pathway after a 85-day FDA review.

K865085 · Van-Tec, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 1987
Decision
85d
Days
Class 2
Risk

K865085 is an FDA 510(k) clearance for the KAMINSKY COMBINATION STENT & INJECTION CATHETER. Classified as Stent, Ureteral (product code FAD), Class II - Special Controls.

Submitted by Van-Tec, Inc. (Spencer, US). The FDA issued a Cleared decision on March 25, 1987 after a review of 85 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4620 - 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 Van-Tec, Inc. devices

FDA 510(k) Submission Details - K865085

510(k) Number K865085 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 30, 1986
Decision Date March 25, 1987
Days to Decision 85 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
46d faster than avg
Panel avg: 131d · This submission: 85d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FAD Device Classification - Class 2, Special Controls

Product Code FAD Stent, Ureteral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4620
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 - FAD Stent, Ureteral

All 104
Devices cleared under the same product code (FAD) and FDA review panel - the closest regulatory comparables to K865085.
MENTOR UNISTENT URETERAL STENT SET
K875038 · Mentor Corp. · Mar 1988
MENTOR BLACK LIGHT URETERAL STENT SET
K873557 · Mentor Corp. · Feb 1988
SURGITEK INFUSION STENT SYSTEM*
K872353 · Surgitek · Sep 1987
ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT
K864225 · Angiomed U.S., Inc. · Jan 1987
METAL TIPPED URETER. STENT & MAGNETIC STENT RETRI.
K863492 · Surgitek · Dec 1986
SILICONE DOUBLE COIL URETERAL STENT WITH SUTURE
K862539 · Mentor Corp. · Sep 1986