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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 K972487
Device Name EMG RETRAINER
Applicant
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
P.O. BOX 489
HIXSON,  TN  37343 -0489
Applicant Contact JOE ELROD
Correspondent
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
P.O. BOX 489
HIXSON,  TN  37343 -0489
Correspondent Contact JOE ELROD
Regulation Number882.5050
Classification Product Code
HCC  
Date Received07/02/1997
Decision Date 09/26/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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