Cleared Traditional

K844280 - TRAVENOL VALUE-LINE URINARY DRAINAGE BAG W/STERILE

K844280 is an FDA 510(k) clearance for TRAVENOL VALUE-LINE URINARY DRAINAGE BA..., manufactured by Travenol Laboratories, S.A.. The device is a Class 2 Gastroenterology & Urology device with product code KNX cleared through the Traditional 510(k) pathway after a 42-day FDA review.

K844280 · Travenol Laboratories, S.A. · Gastroenterology & Urology device
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Dec 1984
Decision
42d
Days
Class 2
Risk

K844280 is an FDA 510(k) clearance for the TRAVENOL VALUE-LINE URINARY DRAINAGE BAG W/STERILE. Classified as Collector, Urine, (and Accessories) For Indwelling Catheter (product code KNX), Class II - Special Controls.

Submitted by Travenol Laboratories, S.A. (Deerfield, US). The FDA issued a Cleared decision on December 17, 1984 after a review of 42 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 Travenol Laboratories, S.A. devices

FDA 510(k) Submission Details - K844280

510(k) Number K844280 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 05, 1984
Decision Date December 17, 1984
Days to Decision 42 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
89d faster than avg
Panel avg: 131d · This submission: 42d
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 102
Devices cleared under the same product code (KNX) and FDA review panel - the closest regulatory comparables to K844280.
ULTRA EXTERNAL CATHETER
K844801 · Inmed Corp. · Jan 1985
COLOPLAST URO 2002 NIGHT DRAINAGE SYSTEM
K844684 · Coloplast A/S · Jan 1985
FEMALE URINARY INCONTINENCE SYS
K843128 · Chesebrough-Pond'S U.S.A. Co. · Jan 1985
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