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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 K873357
Device Name ELECTROBLOC TRANS. ELECTRICAL NERVE BLOCK GENERA.
Applicant
Th Charters, Inc.
9985 SW Heather Ln.
Beaverton,  OR  97008 -6011
Applicant Contact THOMAS H CHARTERS
Correspondent
Th Charters, Inc.
9985 SW Heather Ln.
Beaverton,  OR  97008 -6011
Correspondent Contact THOMAS H CHARTERS
Regulation Number882.5890
Classification Product Code
GZJ  
Date Received08/20/1987
Decision Date 10/26/1987
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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