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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrode, Depth
510(k) Number K902976
Device Name MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC
Applicant
Medical Consultants Intl. , Ltd.
59 Oxford Place
Glen Rock,  NJ  07452
Applicant Contact SAUL LISS
Correspondent
Medical Consultants Intl. , Ltd.
59 Oxford Place
Glen Rock,  NJ  07452
Correspondent Contact SAUL LISS
Regulation Number882.1330
Classification Product Code
GZL  
Date Received07/06/1990
Decision Date 09/07/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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