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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Laparoscope, General & Plastic Surgery
510(k) Number K173822
Device Name Anchor Tissue Retrieval System by CONMED
Applicant
Conmed Corporation
525 French Road
Utica,  NY  13502
Applicant Contact Rachelle D Fitzgerald
Correspondent
Conmed Corporation
525 French Road
Utica,  NY  13502
Correspondent Contact Rachelle D Fitzgerald
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received12/18/2017
Decision Date 09/11/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Obstetrics/Gynecology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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