Cleared Traditional

K811469 - MMG URINARY DRAINAGE TUBING

K811469 is an FDA 510(k) clearance for MMG URINARY DRAINAGE TUBING, manufactured by Medical Marketing Group. The device is a Class 2 Gastroenterology & Urology device with product code KNX cleared through the Traditional 510(k) pathway after a 17-day FDA review.

K811469 · Medical Marketing Group · Gastroenterology & Urology device
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Jun 1981
Decision
17d
Days
Class 2
Risk

K811469 is an FDA 510(k) clearance for the MMG URINARY DRAINAGE TUBING. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by Medical Marketing Group (Decatur, US). The FDA issued a Cleared decision on June 12, 1981 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 876.5250 - 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 Medical Marketing Group devices

FDA 510(k) Submission Details - K811469

510(k) Number K811469 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 26, 1981
Decision Date June 12, 1981
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
114d faster than avg
Panel avg: 131d · This submission: 17d
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 K811469.
CURITY BEDSIDE DRAINAGE BAG
K813621 · The Kendal Co. · Feb 1982
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