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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Nerve, Transcutaneous, For Pain Relief
510(k) Number K896226
Device Name LISS BODY STIMULATOR MODEL SBL501-M
Applicant
Medical Consultants Intl. , Ltd.
59 Oxford Pl.
Glen Rock,  NJ  07452
Applicant Contact SAUL LISS
Correspondent
Medical Consultants Intl. , Ltd.
59 Oxford Pl.
Glen Rock,  NJ  07452
Correspondent Contact SAUL LISS
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received10/31/1989
Decision Date 04/10/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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