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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name device, biofeedback
510(k) Number K941938
Device Name THE MIRAGE SYSTEM BIOFEEDBACK INTERFACE
Applicant
INTERCARE DIAGNOSTICS, INC.
1601 CENTINELA AVE.
SUITE 5
INGLEWOOD,  CA  90302
Applicant Contact ANTHONY DIKE
Correspondent
INTERCARE DIAGNOSTICS, INC.
1601 CENTINELA AVE.
SUITE 5
INGLEWOOD,  CA  90302
Correspondent Contact ANTHONY DIKE
Regulation Number882.5050
Classification Product Code
HCC  
Date Received04/21/1994
Decision Date 08/05/1994
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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