Cleared Traditional

OES ELITE Telescopes, Protective Tube

K151191 · Olympus Winter & Ibe GmbH · Gastroenterology & Urology
Nov 2015
Decision
204d
Days
Class 2
Risk

About This 510(k) Submission

K151191 is an FDA 510(k) clearance for the OES ELITE Telescopes, Protective Tube, a Telescope, Rigid, Endoscopic (Class II — Special Controls, product code FBP), submitted by Olympus Winter & Ibe GmbH (Hamburg, DE). The FDA issued a Cleared decision on November 24, 2015, 204 days after receiving the submission on May 4, 2015. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K151191 FDA.gov
FDA Decision Cleared SESE
Date Received May 04, 2015
Decision Date November 24, 2015
Days to Decision 204 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FBP — Telescope, Rigid, Endoscopic
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500

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