Cleared Traditional

K941851 - DUAL LUMEN CATHETER (DLC) TRAY

K941851 is an FDA 510(k) clearance for DUAL LUMEN CATHETER (DLC) TRAY, manufactured by Neostar Medical Technologies, Inc.. The device is a Class 2 Gastroenterology & Urology device with product code KOC cleared through the Traditional 510(k) pathway after a 333-day FDA review.

K941851 · Neostar Medical Technologies, Inc. · Gastroenterology & Urology device
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Mar 1995
Decision
333d
Days
Class 2
Risk

K941851 is an FDA 510(k) clearance for the DUAL LUMEN CATHETER (DLC) TRAY. Classified as Accessories, Blood Circuit, Hemodialysis (product code KOC), Class II - Special Controls.

Submitted by Neostar Medical Technologies, Inc. (New Brunswick, US). The FDA issued a Cleared decision on March 13, 1995 after a review of 333 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5820 - 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. Elevated predicate reliance profile. 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 Neostar Medical Technologies, Inc. devices

FDA 510(k) Submission Details - K941851

510(k) Number K941851 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 14, 1994
Decision Date March 13, 1995
Days to Decision 333 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
203d slower than avg
Panel avg: 130d · This submission: 333d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KOC Device Classification - Class 2, Special Controls

Product Code KOC Accessories, Blood Circuit, Hemodialysis
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5820
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 - KOC Accessories, Blood Circuit, Hemodialysis

All 123
Devices cleared under the same product code (KOC) and FDA review panel - the closest regulatory comparables to K941851.
ARTERIAL BLOOD TUBING SET FOR SINGLE NEEDLE HEMODIALYSIS
K955277 · Baxter Healthcare Corp · Feb 1996
DIALYSIS ADMINISTRATION KITS
K952572 · B.Braun Medical, Inc. · Jan 1996
KARL STORZ MODIFIED VERESS NEEDLE AND CANNULA
K950282 · KARL STORZ Endoscopy-America, Inc. · Apr 1995
SILICONE CATHETER REPAIR KITS
K926374 · Akcess Medical Products, Inc. · Oct 1994
BARD UROTRACK II MONITORING
K924436 · C.R. Bard, Inc. · Mar 1994
RS-1000
K911230 · Cp Medical · Jun 1993