Cleared Traditional

K030209 - MAHURKAR OPLUS CATHETER

K030209 is an FDA 510(k) clearance for MAHURKAR OPLUS CATHETER, manufactured by The Kendall Company. The device is a Class 2 Gastroenterology & Urology device with product code MPB cleared through the Traditional 510(k) pathway after a 112-day FDA review.

K030209 · The Kendall Company · Gastroenterology & Urology device
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May 2003
Decision
112d
Days
Class 2
Risk

K030209 is an FDA 510(k) clearance for the MAHURKAR OPLUS CATHETER, MODEL 13.5 FR. Classified as Catheter, Hemodialysis, Non-implanted (product code MPB), Class II - Special Controls.

Submitted by The Kendall Company (Mansfield, US). The FDA issued a Cleared decision on May 13, 2003 after a review of 112 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

FDA 510(k) Submission Details - K030209

510(k) Number K030209 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 21, 2003
Decision Date May 13, 2003
Days to Decision 112 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
18d faster than avg
Panel avg: 130d · This submission: 112d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

MPB Device Classification - Class 2, Special Controls

Product Code MPB Catheter, Hemodialysis, Non-implanted
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5540
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 - MPB Catheter, Hemodialysis, Non-implanted

All 29
Devices cleared under the same product code (MPB) and FDA review panel - the closest regulatory comparables to K030209.
NIAGARA, NIAGARA SLIM-CATH, AND BREVIA SHORT-TERM CURVED EXTENSION HEMODIALYSIS CATHETERS
K090102 · C.R. Bard, Inc. · Feb 2009
NIPRO SAFETOUCH TULIP SAFETY FISTULA NEEDLE
K071145 · Nipro Medical Corporation · Sep 2007
NIAGARA TEMPORARY DUAL LUMEN CATHETERS
K030268 · C.R. Bard, Inc. · Jul 2003
NIAGARA SLIM-CATH
K010778 · C.R. Bard, Inc. · Apr 2001
14 FR TWO-LUMEN HEMODIALYSIS CATHERIZATION KIT WITH BLUE FLEXTIP ARROWG+ARD BLUE CATHETER FOR HIGH VOLUME INFUSIONS, PRO
K993933 · Arrow Intl., Inc. · Sep 2000
MEDCOMP DUO-FLOW II CATHETER WITH LUBRICIOUS HEPARIN
K991320 · Medical Components, Inc. · Nov 1999