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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Interferential Current Therapy
510(k) Number K904743
Device Name LSI SYSTEM II
Applicant
M.S.P. , Ltd.
8851 Bond
Overland Park,  KS  66214
Applicant Contact STEVE PAPA
Correspondent
M.S.P. , Ltd.
8851 Bond
Overland Park,  KS  66214
Correspondent Contact STEVE PAPA
Regulation Number882.5890
Classification Product Code
LIH  
Date Received10/18/1990
Decision Date 09/04/1991
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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