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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Anesthesia Conduction Kit
510(k) Number K894725
Device Name MEDIZIV EPIDURAL SYSTEMS
Applicant
Mediziv Medical Devices, Ltd.
88, Weizman St.
Tel-Aviv
Israel,  IL 62264
Applicant Contact SAMUEL BAR-ZIV
Correspondent
Mediziv Medical Devices, Ltd.
88, Weizman St.
Tel-Aviv
Israel,  IL 62264
Correspondent Contact SAMUEL BAR-ZIV
Regulation Number868.5140
Classification Product Code
CAZ  
Date Received07/25/1989
Decision Date 10/13/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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