Cleared Traditional

K903611 - ILC LEG BAG HOLDER

K903611 is an FDA 510(k) clearance for ILC LEG BAG HOLDER, manufactured by Inman Liebelt Corp.. The device is a Class 1 Gastroenterology & Urology device with product code FAQ cleared through the Traditional 510(k) pathway after a 78-day FDA review.

K903611 · Inman Liebelt Corp. · Gastroenterology & Urology device
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Oct 1990
Decision
78d
Days
Class 1
Risk

K903611 is an FDA 510(k) clearance for the ILC LEG BAG HOLDER. Classified as Bag, Urine Collection, Leg, For External Use, Sterile (product code FAQ), Class I - General Controls.

Submitted by Inman Liebelt Corp. (Arlington, US). The FDA issued a Cleared decision on October 26, 1990 after a review of 78 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 Inman Liebelt Corp. devices

FDA 510(k) Submission Details - K903611

510(k) Number K903611 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 09, 1990
Decision Date October 26, 1990
Days to Decision 78 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
52d faster than avg
Panel avg: 130d · This submission: 78d
Pathway characteristics
Predicate-based equivalence.

FAQ Device Classification - Class 1, General Controls

Product Code FAQ Bag, Urine Collection, Leg, For External Use, Sterile
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.5250
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - FAQ Bag, Urine Collection, Leg, For External Use, Sterile

All 10
Devices cleared under the same product code (FAQ) and FDA review panel - the closest regulatory comparables to K903611.
PROSYS LEG BAG
K951945 · Convatec, A Division of E.R. Squibb & Sons · May 1995
BARD LEG BAG HOLDER
K926035 · C.R. Bard, Inc. · Dec 1992
CONVEEN(R) LEG BAG(500 ML)
K924406 · Coloplast A/S · Oct 1992
EXTERNAL LEG BAG
K901219 · Orion Life Systems, Inc. · Jun 1990
QUADRIPLEGIC URINARY DRAINAGE VALVE
K772402 · Fred Sammons, Inc. · Jan 1978
URINARY LEG BAG
K780032 · C.R. Bard, Inc. · Jan 1978