FDA 510(k) Application Details - K073154

Device Classification Name	Dynamometer, Ac-Powered   More FDA Info for this Device
510(K) Number	K073154
Device Name	Dynamometer, Ac-Powered
Applicant	GLOBAL SERVICES GROUP, LLC 350 MCLAWS CIRCLE SUITE 2 WILLIAMSBURG, VA 23185 US Other 510(k) Applications for this Company
Contact	RAY GAGNE Other 510(k) Applications for this Contact
Regulation Number	888.1240   More FDA Info for this Regulation Number
Classification Product Code	LBB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/08/2007
Decision Date	02/14/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	NE - Neurology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review