Cleared Special

K043272 - PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER WITH SLOTTED SYMMETRICAL TIP
(FDA 510(k) Clearance)

Dec 2004
Decision
26d
Days
Class 2
Risk

K043272 is an FDA 510(k) clearance for the PALLINDROME 14.5FR CHRONIC HEMODIALYSIS CATHETER WITH SLOTTED SYMMETRICAL TIP. This device is classified as a Catheter, Hemodialysis, Implanted (Class II - Special Controls, product code MSD).

Submitted by Kendall (Mansfield, US). The FDA issued a Cleared decision on December 22, 2004, 26 days after receiving the submission on November 26, 2004.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5540.

Submission Details

510(k) Number K043272 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 26, 2004
Decision Date December 22, 2004
Days to Decision 26 days
Submission Type Special
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code MSD — Catheter, Hemodialysis, Implanted
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5540

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