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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Goniometer, Ac-Powered
510(k) Number K812908
Device Name ELECTRO-GONIOMETER
Applicant
CHATTANOOGA GROUP, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
CHATTANOOGA GROUP, INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number888.1500
Classification Product Code
KQX  
Date Received10/19/1981
Decision Date 11/24/1981
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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