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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 K931321
Device Name CSD 200/300/400/500 DYNAMOMETER
Applicant
JOHN CHATILLON & SONS, INC.
P.O. BOX 35668
GREENSBORO,  NC  27425 -5668
Applicant Contact KAMPERMAN
Correspondent
JOHN CHATILLON & SONS, INC.
P.O. BOX 35668
GREENSBORO,  NC  27425 -5668
Correspondent Contact KAMPERMAN
Regulation Number888.1240
Classification Product Code
LBB  
Date Received03/16/1993
Decision Date 02/15/1994
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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