Cleared Traditional

K925659 - U.C.E.Z. LENS CLEANER KIT
(FDA 510(k) Clearance)

Sep 1993
Decision
345d
Days
Class 2
Risk

K925659 is an FDA 510(k) clearance for the U.C.E.Z. LENS CLEANER KIT. This device is classified as a Anti Fog Solution And Accessories, Endoscopy (Class II - Special Controls, product code OCT).

Submitted by Anago, Inc. (Fort Worth, US). The FDA issued a Cleared decision on September 17, 1993, 345 days after receiving the submission on October 7, 1992.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Prevent, Reduce Or Eliminate Condensation (fog) On Endoscopic Lens..

Submission Details

510(k) Number K925659 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 07, 1992
Decision Date September 17, 1993
Days to Decision 345 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement

Device Classification

Product Code OCT — Anti Fog Solution And Accessories, Endoscopy
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Prevent, Reduce Or Eliminate Condensation (fog) On Endoscopic Lens.

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