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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 K923262
Device Name DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER
Applicant
John Chatillon & Sons, Inc.
P.O. Box 35668
Greensboro,  NC  27425
Applicant Contact E. F KAMPERMAN
Correspondent
John Chatillon & Sons, Inc.
P.O. Box 35668
Greensboro,  NC  27425
Correspondent Contact E. F KAMPERMAN
Regulation Number888.1240
Classification Product Code
LBB  
Date Received07/02/1992
Decision Date 10/27/1992
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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