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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
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