Cleared Traditional

FOLEY CATHETERS WITH TEMPERATURE PROBE

K061918 · Ge Healthcare · Gastroenterology & Urology
Aug 2006
Decision
43d
Days
Class 2
Risk

About This 510(k) Submission

K061918 is an FDA 510(k) clearance for the FOLEY CATHETERS WITH TEMPERATURE PROBE, a Catheter, Upper Urinary Tract (Class II — Special Controls, product code EYC), submitted by Ge Healthcare (Needham, US). The FDA issued a Cleared decision on August 18, 2006, 43 days after receiving the submission on July 6, 2006. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5130.

Submission Details

510(k) Number K061918 FDA.gov
FDA Decision Cleared SESE
Date Received July 06, 2006
Decision Date August 18, 2006
Days to Decision 43 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code EYC — Catheter, Upper Urinary Tract
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5130