Cleared Traditional

K020936 - 10F X 18CM PEDIATRIC ASH SPLIT CATH XL

Also marketed or referenced as:
10F X 24CM PEDIATRIC ASH SPLIT-CATH XL, MODEL ASPC24P-XL

K020936 is the FDA 510(k) clearance for 10F X 18CM PEDIATRIC ASH SPLIT CATH XL by Medcomp. It is a Class 2 Gastroenterology & Urology device (product code MSD) cleared through the Traditional 510(k) pathway after a 203-day FDA review.

K020936 · Medcomp · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Oct 2002
Decision
203d
Days
Class 2
Risk

K020936 is an FDA 510(k) clearance for the 10F X 18CM PEDIATRIC ASH SPLIT CATH XL, MODEL ASPC18P-XL. Classified as Catheter, Hemodialysis, Implanted (product code MSD), Class II - Special Controls.

Submitted by Medcomp (Harleysville, US). The FDA issued a Cleared decision on October 11, 2002 after a review of 203 days - an extended review cycle.

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 Medcomp devices

Submission Details

510(k) Number K020936 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received March 22, 2002
Decision Date October 11, 2002
Days to Decision 203 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
73d slower than avg
Panel avg: 130d · This submission: 203d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MSD Catheter, Hemodialysis, 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 - MSD Catheter, Hemodialysis, Implanted

All 42
Devices cleared under the same product code (MSD) and FDA review panel - the closest regulatory comparables to K020936.
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HEMOSPLIT LONG-TERM HEMODIALYSIS CATHETER
K030020 · C.R. Bard, Inc. · Jun 2003
DIATEK CANNON-CATHETER, MODEL CC5500
K022662 · Arrow Intl., Inc. · May 2003
VAXCEL DIALYSIS CATHETER
K012365 · Boston Scientific Corp · Aug 2001
OPTIFLOW CATHETER #5641190 CATHETER ONLY #5643150 CATHETER KIT #5631000 CATHETERLESS TRAY-GENERIC (COMBINED WITH CATHETR
K010567 · C.R. Bard, Inc. · Mar 2001
MEDI-TECH DIALYSIS CATHETER GASTROENTEROLOGY
K982326 · Boston Scientific Corp · Jul 1999