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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 K924490
Device Name MASTERSTIM I-2
Applicant
HEALTH CARE ASSOC.
2146 E. PYTHIAN
SPRINGFIELD,  MO  65802
Applicant Contact JACK BALES
Correspondent
HEALTH CARE ASSOC.
2146 E. PYTHIAN
SPRINGFIELD,  MO  65802
Correspondent Contact JACK BALES
Regulation Number882.5890
Classification Product Code
LIH  
Date Received09/03/1992
Decision Date 02/05/1993
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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