Cleared Traditional

K810367 - KISH URETHRAL ILLUMINATED CATHETER SET

K810367 is the FDA 510(k) clearance for KISH URETHRAL ILLUMINATED CATHETER SET by Vance Products, Inc.. It is a Class 2 Gastroenterology & Urology device (product code KOD) cleared through the Traditional 510(k) pathway after a 36-day FDA review.

K810367 · Vance Products, Inc. · Gastroenterology & Urology device
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Mar 1981
Decision
36d
Days
Class 2
Risk

K810367 is an FDA 510(k) clearance for the KISH URETHRAL ILLUMINATED CATHETER SET. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Vance Products, Inc. (Walker, US). The FDA issued a Cleared decision on March 20, 1981 after a review of 36 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5130 - 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 Vance Products, Inc. devices

Submission Details

510(k) Number K810367 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 12, 1981
Decision Date March 20, 1981
Days to Decision 36 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
94d faster than avg
Panel avg: 130d · This submission: 36d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code KOD Catheter, Urological
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5130
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 - KOD Catheter, Urological

All 125
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K810367.
PRE-FILLED SYRINGE & CYSTOFLO URINARY BG
K811924 · Travenol Laboratories, S.A. · Nov 1981
CURITY 100% SILICONE SAFETY INDICATOR
K810690 · The Kendal Co. · Apr 1981
SILICONE ELASTOMER COATED LATEX FOLEY
K810630 · G.D. Searle and Co. · Mar 1981
ARGYLE ROB-NELS
K810216 · Sherwood Medical Co. · Feb 1981
CLOSED SYSTEM URETHRAL CATHETERIZ. SET
K803259 · Medical Devices, Inc. · Jan 1981
FOLEY CATHETER
K803079 · American Hospital Supply Corp. · Dec 1980