Cleared Traditional

K043418 - COOK PEDIATRIC FLEXOR URETERAL ACCESS SHEALTH
(FDA 510(k) Clearance)

K043418 · Cook Urological, Inc. · Gastroenterology & Urology
Mar 2005
Decision
108d
Days
Class 2
Risk

K043418 is an FDA 510(k) clearance for the COOK PEDIATRIC FLEXOR URETERAL ACCESS SHEALTH. This device is classified as a Endoscopic Access Overtube, Gastroenterology-urology (Class II — Special Controls, product code FED).

Submitted by Cook Urological, Inc. (Spencer, US). The FDA issued a Cleared decision on March 31, 2005, 108 days after receiving the submission on December 13, 2004.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation..

Submission Details

510(k) Number K043418 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 13, 2004
Decision Date March 31, 2005
Days to Decision 108 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FED — Endoscopic Access Overtube, Gastroenterology-urology
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Facilitate Passage And Aid Advancement Of Endoscopes Into The Body, Especially In Cases Of Repeated Intubation.

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