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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 K792659
Device Name FEEDBACK EDR SYSTEM MODEL ME-1
Applicant
BIO-FEEDBACK SYSTEMS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
BIO-FEEDBACK SYSTEMS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number882.5050
Classification Product Code
HCC  
Date Received12/26/1979
Decision Date 01/09/1980
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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