Cleared Traditional

K803080 - ALL PUPOSE URETHRAL CATHETER

K803080 is the FDA 510(k) clearance for ALL PUPOSE URETHRAL CATHETER by American Hospital Supply Corp.. It is a Class 2 Gastroenterology & Urology device (product code KOD) cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K803080 · American Hospital Supply Corp. · Gastroenterology & Urology device
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Dec 1980
Decision
17d
Days
Class 2
Risk

K803080 is an FDA 510(k) clearance for the ALL PUPOSE URETHRAL CATHETER. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by American Hospital Supply Corp. (Mchenry, US). The FDA issued a Cleared decision on December 22, 1980 after a review of 17 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 American Hospital Supply Corp. devices

Submission Details

510(k) Number K803080 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 05, 1980
Decision Date December 22, 1980
Days to Decision 17 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
113d faster than avg
Panel avg: 130d · This submission: 17d
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 80
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K803080.
ROBINSON CATHETERS NON-STERILE
K812887 · Abco Dealers, Inc. · Nov 1981
PRE-FILLED SYRINGE & CYSTOFLO URINARY BG
K811924 · Travenol Laboratories, S.A. · Nov 1981
ARGYLE ROB-NELS
K810216 · Sherwood Medical Co. · Feb 1981
ARGYLE HEMATURIA BALLOON CATHETER
K802875 · Sherwood Medical Co. · Dec 1980
FOLEY CATHETER
K802516 · Abco Dealers, Inc. · Oct 1980
FOLEY CATHETERIZATION TRAY
K801820 · Abco Dealers, Inc. · Oct 1980