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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 K924961
Device Name HMP 4000 INTERFERENTIAL STIMULATOR
Applicant
Hmp 4000, Inc.
10901 Red Cir. Dr. #150
Minnetonka,  MN  55343
Applicant Contact SCOTT R ANDERSON
Correspondent
Hmp 4000, Inc.
10901 Red Cir. Dr. #150
Minnetonka,  MN  55343
Correspondent Contact SCOTT R ANDERSON
Regulation Number882.5890
Classification Product Code
LIH  
Date Received09/30/1992
Decision Date 02/25/1993
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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