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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Imaging, Gastrointestinal, Wireless, Capsule
510(k) Number K022362
Device Name GIVEN DIAGNOSTICS SYSTEM
Applicant
Given Imaging , Ltd.
New Industrial Park
P.O. Box 258
Yoqneaam,  IL 20692
Applicant Contact SHOSHANA FRIEDMAN
Correspondent
Given Imaging , Ltd.
New Industrial Park
P.O. Box 258
Yoqneaam,  IL 20692
Correspondent Contact SHOSHANA FRIEDMAN
Regulation Number876.1300
Classification Product Code
NEZ  
Date Received07/22/2002
Decision Date 08/09/2002
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Gastroenterology/Urology
510k Review Panel Gastroenterology/Urology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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