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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 K954951
Device Name TAYLOR GENERAL PURPOSE MONITORING ELECTRODE
Applicant
TAYLOR INDUSTRIES, INC.
2995 SOUTH MOORLAND RD.
NEW BERLIN,  WI  53151
Applicant Contact MICHAEL BALLARD
Correspondent
TAYLOR INDUSTRIES, INC.
2995 SOUTH MOORLAND RD.
NEW BERLIN,  WI  53151
Correspondent Contact MICHAEL BALLARD
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received10/30/1995
Decision Date 05/30/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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