Cleared Traditional

K802083 - CATHETER INSERTION TRAY

K802083 is the FDA 510(k) clearance for CATHETER INSERTION TRAY by Walpak Co.. It is a Class 2 Gastroenterology & Urology device (product code KOD) cleared through the Traditional 510(k) pathway after a 18-day FDA review.

K802083 · Walpak Co. · Gastroenterology & Urology device
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Sep 1980
Decision
18d
Days
Class 2
Risk

K802083 is an FDA 510(k) clearance for the CATHETER INSERTION TRAY. Classified as Catheter, Urological (product code KOD), Class II - Special Controls.

Submitted by Walpak Co. (Mchenry, US). The FDA issued a Cleared decision on September 16, 1980 after a review of 18 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 Walpak Co. devices

Submission Details

510(k) Number K802083 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 29, 1980
Decision Date September 16, 1980
Days to Decision 18 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
112d faster than avg
Panel avg: 130d · This submission: 18d
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 128
Devices cleared under the same product code (KOD) and FDA review panel - the closest regulatory comparables to K802083.
URINARY CATHETER CARE TRAYS #3700&3710
K801787 · The Healthcare Group Laboratories, Inc. · Oct 1980
FOLEY CATHETERIZATION TRAY
K801820 · Abco Dealers, Inc. · Oct 1980
URINE COLLECTION CONTAINERS, #3600 &3610
K801786 · The Healthcare Group Laboratories, Inc. · Sep 1980
LATEX FOLEY CATHETER (HYDROMER COATED)
K801415 · G.D. Searle and Co. · Aug 1980
URINARY CATHETERS #3400,3410 &3420
K801784 · The Healthcare Group Laboratories, Inc. · Aug 1980
CATHETER STYLET
K800609 · G.D. Searle and Co. · Apr 1980