Cleared Traditional

K012074 - XBO1-824-18/19/20 BIOPSY FORCEPS
(FDA 510(k) Clearance)

Sep 2001
Decision
85d
Days
Class 2
Risk

K012074 is an FDA 510(k) clearance for the XBO1-824-18/19/20 BIOPSY FORCEPS. This device is classified as a Endoscopic Grasping/cutting Instrument, Non-powered (Class II - Special Controls, product code OCZ).

Submitted by The Olympus Optical Co. (Melville, US). The FDA issued a Cleared decision on September 25, 2001, 85 days after receiving the submission on July 2, 2001.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.1500. To Manually Grasp Stones, Tissues Or Other Objects Through An Endoscope. To Manipulate, Sample Or Cut Tissues Through An Endoscope..

Submission Details

510(k) Number K012074 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 02, 2001
Decision Date September 25, 2001
Days to Decision 85 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code OCZ — Endoscopic Grasping/cutting Instrument, Non-powered
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Manually Grasp Stones, Tissues Or Other Objects Through An Endoscope. To Manipulate, Sample Or Cut Tissues Through An Endoscope.

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