Cleared Traditional

Grasping Forceps

K152802 · Micro-Tech (Nanjing) Co., Ltd. · Gastroenterology & Urology
Jan 2016
Decision
115d
Days
Class 2
Risk

About This 510(k) Submission

K152802 is an FDA 510(k) clearance for the Grasping Forceps, a Endoscopic Grasping/cutting Instrument, Non-powered (Class II — Special Controls, product code OCZ), submitted by Micro-Tech (Nanjing) Co., Ltd. (Nanjing, CN). The FDA issued a Cleared decision on January 21, 2016, 115 days after receiving the submission on September 28, 2015. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K152802 FDA.gov
FDA Decision Cleared SESE
Date Received September 28, 2015
Decision Date January 21, 2016
Days to Decision 115 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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