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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 K180579
Device Name Ezee Retrieval
Applicant
Genicon, Inc.
6869 Stapoint Ct.
Suite 114
Winter Park,  FL  32792
Applicant Contact Katlyn Kachman
Correspondent
Genicon, Inc.
6869 Stapoint Ct.
Suite 114
Winter Park,  FL  32792
Correspondent Contact Katlyn Kachman
Regulation Number876.1500
Classification Product Code
GCJ  
Date Received03/05/2018
Decision Date 03/19/2018
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel General & Plastic Surgery
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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