Cleared Traditional

K802664 - URINARY DRAINAGE UNT

K802664 is an FDA 510(k) clearance for URINARY DRAINAGE UNT, manufactured by Diamed Division Ill. Tool Works, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KNX cleared through the Traditional 510(k) pathway after a 15-day FDA review.

K802664 · Diamed Division Ill. Tool Works, Inc. · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Nov 1980
Decision
15d
Days
Class 2
Risk

K802664 is an FDA 510(k) clearance for the URINARY DRAINAGE UNT. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by Diamed Division Ill. Tool Works, Inc. (Mchenry, US). The FDA issued a Cleared decision on November 12, 1980 after a review of 15 days - a notably fast clearance cycle.

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: 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 Diamed Division Ill. Tool Works, Inc. devices

FDA 510(k) Submission Details - K802664

510(k) Number K802664 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 28, 1980
Decision Date November 12, 1980
Days to Decision 15 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
116d faster than avg
Panel avg: 131d · This submission: 15d
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 103
Devices cleared under the same product code (KNX) and FDA review panel - the closest regulatory comparables to K802664.
HOLLISTER FEMALE URINARY COLLECT SYS
K820234 · Hollister, Inc. · Feb 1982
ARGYLE PEDIATRIC URINE COLLECTOR
K813479 · Sherwood Medical Co. · Jan 1982
ARGYLE CLOSED URINARY DRAINAGE SET
K802667 · Sherwood Medical Co. · Dec 1980
BARD MALE EXTERNAL CATHETER
K802433 · C.R. Bard, Inc. · Oct 1980
LEG BAG EXTENSION TUBE
K802606 · Associated Medical Products Co. · Oct 1980
URIHESIVE SYSTEM
K802172 · E. R. Squibb & Sons, Inc. · Sep 1980