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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name goniometer, nonpowered
510(k) Number K850082
Device Name HAND HELD GONIOMETER
Applicant
CHATTANOOGA GROUP, INC.
101 MEMORIAL DR.
RED BANK,  TN  37405
Applicant Contact MALEY
Correspondent
CHATTANOOGA GROUP, INC.
101 MEMORIAL DR.
RED BANK,  TN  37405
Correspondent Contact MALEY
Regulation Number888.1520
Classification Product Code
KQW  
Date Received01/10/1985
Decision Date 04/04/1985
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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