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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Dynamometer, Ac-Powered
510(k) Number K901290
Device Name ELECTRO-GONIOMETER DIAGNOSTIC DEVICE
Applicant
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
P.O. BOX 4287
HIXSON,  TN  37343
Applicant Contact GRAHAME R WATTS
Correspondent
CHATTANOOGA GROUP, INC.
4717 ADAMS RD.
P.O. BOX 4287
HIXSON,  TN  37343
Correspondent Contact GRAHAME R WATTS
Regulation Number888.1240
Classification Product Code
LBB  
Date Received03/20/1990
Decision Date 10/01/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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