Cleared Traditional

NORTHGATE FLOW ASSIST TUBING FOR UROLOGY

K943361 · Northgate Technologies, Inc. · Gastroenterology & Urology
Sep 1995
Decision
443d
Days
Class 2
Risk

About This 510(k) Submission

K943361 is an FDA 510(k) clearance for the NORTHGATE FLOW ASSIST TUBING FOR UROLOGY, a System, Irrigation, Urological (Class II — Special Controls, product code LJH), submitted by Northgate Technologies, Inc. (Arlington Heights, US). The FDA issued a Cleared decision on September 29, 1995, 443 days after receiving the submission on July 13, 1994. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5130.

Submission Details

510(k) Number K943361 FDA.gov
FDA Decision Cleared SESE
Date Received July 13, 1994
Decision Date September 29, 1995
Days to Decision 443 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement

Device Classification

Product Code LJH — System, Irrigation, Urological
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5130

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