Cleared Traditional

MAHURKAR TRIPLE LUMEN CATHETER, 12 FR (K020089) - FDA 510(k) Clearance

Class II Gastroenterology & Urology device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K020089 · The Kendall Company · Gastroenterology & Urology device
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Apr 2002
Decision
90d
Days
Class 2
Risk

K020089 is an FDA 510(k) clearance for the MAHURKAR TRIPLE LUMEN CATHETER, 12 FR. Classified as Catheter, Hemodialysis, Triple Lumen, Non-implanted (product code NIE), Class II - Special Controls.

Submitted by The Kendall Company (Mansfield, US). The FDA issued a Cleared decision on April 10, 2002 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5540 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all The Kendall Company devices

Submission Details

510(k) Number K020089 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 10, 2002
Decision Date April 10, 2002
Days to Decision 90 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
40d faster than avg
Panel avg: 130d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code NIE Catheter, Hemodialysis, Triple Lumen, Non-implanted
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5540
Definition Short-term (< 30 Days) Central Venous Access For Hemodialysis And Apheresis, With A Third Lumen For Infusion.
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 - NIE Catheter, Hemodialysis, Triple Lumen, Non-implanted

All 11
Devices cleared under the same product code (NIE) and FDA review panel - the closest regulatory comparables to K020089.
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K232945 · Medical Components, Inc. (dba MedComp) · Nov 2023
Power Acute Triple Lumen Hemodialysis Catheter
K222170 · Health Line International Corporation · Jan 2023
Trio-CT Triple Lumen Catheter
K183219 · Medical Components, Inc. (dba MedComp) · Jun 2019
12F Tri-Flow Triple Lumen Catheter
K181175 · Medical Components, Inc. (dba MedComp) · Jul 2018
POWER-TRIALYSIS SLIM-CATH SHORT-TERM DIALYSIS CATHETER
K141531 · C.R. Bard, Inc. · Jun 2015
POWER-TRIALYSIS SHORT-TERM DIALYSIS CATHETER
K133456 · C.R. Bard, Inc. · Sep 2014