Cleared Traditional

K896053 - ALL SILICONE FOLEY CATHETER

K896053 is an FDA 510(k) clearance for ALL SILICONE FOLEY CATHETER, manufactured by Rochester Medical Corp.. The device is a Class 2 Gastroenterology & Urology device with product code KOD cleared through the Traditional 510(k) pathway after a 117-day FDA review.

K896053 · Rochester Medical Corp. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Feb 1990
Decision
117d
Days
Class 2
Risk

K896053 is an FDA 510(k) clearance for the ALL SILICONE FOLEY CATHETER. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Rochester Medical Corp. (Rochester, US). The FDA issued a Cleared decision on February 12, 1990 after a review of 117 days - within the typical 510(k) review window.

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: 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 Rochester Medical Corp. devices

FDA 510(k) Submission Details - K896053

510(k) Number K896053 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 18, 1989
Decision Date February 12, 1990
Days to Decision 117 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
14d faster than avg
Panel avg: 131d · This submission: 117d
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 151
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K896053.
PHARMASEAL DISPOSABLE ABDOMINAL TROCAR
K904734 · Baxter Healthcare Corp · Nov 1990
BARD CONFORMACATH FOLEY CATHETER
K900229 · C.R. Bard, Inc. · Apr 1990
DISPOSABLE URODYNAMIC CATHETER SET
K896784 · Life-Tech Intl., Inc. · Feb 1990
CONVEEN INTERMITTENT CATHETERS
K895548 · Coloplast A/S · Feb 1990
CYSTO PUMP DRAINAGE BAG
K896208 · Westmark, Sterile Packing Systems, Inc. (Sps) · Jan 1990
CYSTOSCOPY/IRRIGATION SET
K896211 · Westmark, Sterile Packing Systems, Inc. (Sps) · Jan 1990