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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 K964685
Device Name DYNAMOMETER
Applicant
John Chatillon & Sons, Inc.
7609 Business Park Dr.
Greensboro,  NC  27409
Applicant Contact JOSEPH R TROY
Correspondent
John Chatillon & Sons, Inc.
7609 Business Park Dr.
Greensboro,  NC  27409
Correspondent Contact JOSEPH R TROY
Regulation Number888.1240
Classification Product Code
LBB  
Date Received11/22/1996
Decision Date 01/27/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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