Cleared Traditional

K843117 - GREEN CROSS URINARY DRAINAGE BAG

K843117 is an FDA 510(k) clearance for GREEN CROSS URINARY DRAINAGE BAG, manufactured by Tech-Cons Ltd., Intl.. The device is a Class 2 Gastroenterology & Urology device with product code KNX cleared through the Traditional 510(k) pathway after a 64-day FDA review.

K843117 · Tech-Cons Ltd., Intl. · Gastroenterology & Urology device
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Oct 1984
Decision
64d
Days
Class 2
Risk

K843117 is an FDA 510(k) clearance for the GREEN CROSS URINARY DRAINAGE BAG. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by Tech-Cons Ltd., Intl. (Chicago, US). The FDA issued a Cleared decision on October 11, 1984 after a review of 64 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 Tech-Cons Ltd., Intl. devices

FDA 510(k) Submission Details - K843117

510(k) Number K843117 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 08, 1984
Decision Date October 11, 1984
Days to Decision 64 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
67d faster than avg
Panel avg: 131d · This submission: 64d
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 K843117.
TRAVENOL VALUE-LINE URINARY DRAINAGE BAG W/STERILE
K844280 · Travenol Laboratories, S.A. · Dec 1984
PHARMA-PLAST URIDROP-URIDOME
K843478 · Zimmar Consulting , Ltd. · Dec 1984
PHARMA-PLAST CONNECTING TUBE TYPE URIN-
K843481 · Zimmar Consulting , Ltd. · Oct 1984
PHARMA-PLAST LEG BAG
K843479 · Zimmar Consulting , Ltd. · Oct 1984
PHARMA-PLAST URINARY DRAINAGE BAG 2000
K843480 · Zimmar Consulting , Ltd. · Oct 1984
CORPAK URINARY DRAINAGE BAG
K842257 · Corpak Co. · Aug 1984