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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 K844994
Device Name THE MEHESZ STIMULATING SYSTEM
Applicant
Campden Medical , Ltd.
186 Campden Hill Rd.
London - W8 7th,  GB
Applicant Contact WEISS
Correspondent
Campden Medical , Ltd.
186 Campden Hill Rd.
London - W8 7th,  GB
Correspondent Contact WEISS
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received12/26/1984
Decision Date 03/06/1985
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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