Cleared Traditional

K914933 - HEART PACK III

K914933 is an FDA 510(k) clearance for HEART PACK III, manufactured by Westmark Hospital Supplies. The device is a Class 2 Gastroenterology & Urology device with product code KOD cleared through the Traditional 510(k) pathway after a 88-day FDA review.

K914933 · Westmark Hospital Supplies · Gastroenterology & Urology device
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Jan 1992
Decision
88d
Days
Class 2
Risk

K914933 is an FDA 510(k) clearance for the HEART PACK III. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Westmark Hospital Supplies (Grand Rapids, US). The FDA issued a Cleared decision on January 31, 1992 after a review of 88 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 Westmark Hospital Supplies devices

FDA 510(k) Submission Details - K914933

510(k) Number K914933 FDA.gov
FDA Decision Cleared Substantially Equivalent - De Novo Granted (SEKD)
Date Received November 04, 1991
Decision Date January 31, 1992
Days to Decision 88 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
42d faster than avg
Panel avg: 130d · This submission: 88d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOD Device Classification - Class 2, Special Controls

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 130
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K914933.
BARD LATEX URINARY CATHETERS
K922431 · C.R. Bard, Inc. · Mar 1993
RADIFOCUS GUIDE WIRE M
K923607 · Terumo Medical Corp. · Oct 1992
KENDALL MOD. PEDIATRIC ULTRAMER POLYURETHANE CATH.
K921054 · Kendall Healthcare Products Co. Div.Of Tyco Health · Sep 1992
NAUDE URETHRAL STENT
K912851 · Cook Urological, Inc. · Jan 1992
KENDALL PEDIATRIC ULTRAMER POLYURETHANE CATHETER
K911242 · Kendall Healthcare Products Co. Div.Of Tyco Health · Apr 1991
PHARMASEAL DISPOSABLE ABDOMINAL TROCAR
K904734 · Baxter Healthcare Corp · Nov 1990