Cleared Traditional

K841169 - CURITY RIG FOLEY CATH TRAY

K841169 is an FDA 510(k) clearance for CURITY RIG FOLEY CATH TRAY, manufactured by The Kendal Co.. The device is a Class 2 Gastroenterology & Urology device with product code KNX cleared through the Traditional 510(k) pathway after a 109-day FDA review.

K841169 · The Kendal Co. · Gastroenterology & Urology device
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Jul 1984
Decision
109d
Days
Class 2
Risk

K841169 is an FDA 510(k) clearance for the CURITY RIG FOLEY CATH TRAY. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by The Kendal Co. (Walker, US). The FDA issued a Cleared decision on July 6, 1984 after a review of 109 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5250 - 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 The Kendal Co. devices

FDA 510(k) Submission Details - K841169

510(k) Number K841169 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 19, 1984
Decision Date July 06, 1984
Days to Decision 109 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
21d faster than avg
Panel avg: 130d · This submission: 109d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNX Device Classification - Class 2, Special Controls

Product Code KNX Collector, Urine, (and Accessories) For Indwelling Catheter
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5250
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 - KNX Collector, Urine, (and Accessories) For Indwelling Catheter

All 85
Devices cleared under the same product code (KNX) and FDA review panel - the closest regulatory comparables to K841169.
CYSTOFLO ANTIMICROBIAL URINARY DRAINAGE
K832290 · Travenol Laboratories, S.A. · Jul 1984
CHESEBROUGH-POND'S REUSABLE URINARY LEG
K842553 · Chesebrough-Pond'S U.S.A. Co. · Jul 1984
CYSTO-AID
K841197 · E-Z-Em, Inc. · Jul 1984
URIHESIVE SYSTEM - IMPROVED
K834337 · Convatec, A Division of E.R. Squibb & Sons · Feb 1984
COLOPLAST BABY URINE COLLECTORS
K833570 · Coloplast A/S · Jan 1984
CLOSED SYS. DRAINAGE BAGS & TRAYS
K832822 · Medline Industries, Inc. · Oct 1983