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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Electrode, Cutaneous
510(k) Number K884348
Device Name MODIFIED JELTRODE(TM) ELECTRODES DEEMED
Applicant
HENLEY INTL.
104 INDUSTRIAL BLVD.,
SUGAR LAND,  TX  77470
Applicant Contact ERNEST J HENLEY
Correspondent
HENLEY INTL.
104 INDUSTRIAL BLVD.,
SUGAR LAND,  TX  77470
Correspondent Contact ERNEST J HENLEY
Regulation Number882.1320
Classification Product Code
GXY  
Date Received10/14/1988
Decision Date 12/15/1988
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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