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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 -9301
Applicant Contact JOSEPH R TROY
Correspondent
JOHN CHATILLON & SONS, INC.
7609 BUSINESS PARK DR.
GREENSBORO,  NC  27409 -9301
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
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