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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name stimulator, ultrasound and muscle, for use in applying therapeutic deep heat
510(k) Number K982830
Device Name FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO
Applicant
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
HIXSON,  TN  37343
Applicant Contact JOE ELROD
Correspondent
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
HIXSON,  TN  37343
Correspondent Contact JOE ELROD
Regulation Number890.5860
Classification Product Code
IMG  
Subsequent Product Codes
GZJ   IMI   IPF   LIH  
Date Received08/11/1998
Decision Date 11/06/1998
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
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