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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 K941561
Device Name FORTE US
Applicant
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 489
Hixson,  TN  37343
Applicant Contact GRAHAME R WATTS
Correspondent
Chattanooga Group, Inc.
4717 Adams Rd.
P.O. Box 489
Hixson,  TN  37343
Correspondent Contact GRAHAME R WATTS
Regulation Number890.5860
Classification Product Code
IMG  
Date Received04/01/1994
Decision Date 06/20/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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