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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 K862718
Device Name VERSA STIM
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501
Applicant Contact WILLIAM ABRAHAM
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501
Correspondent Contact WILLIAM ABRAHAM
Regulation Number882.1320
Classification Product Code
GXY  
Date Received07/17/1986
Decision Date 09/09/1986
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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