FDA 510(k) Application Details - K981730

Device Classification Name	Dynamometer, Ac-Powered   More FDA Info for this Device
510(K) Number	K981730
Device Name	Dynamometer, Ac-Powered
Applicant	NK BIOTECHNICAL CORP. 10850 OLD COUNTY RD. 15 MINNEAPOLIS, MN 55441 US Other 510(k) Applications for this Company
Contact	KAREN GOTFREDSON 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	05/15/1998
Decision Date	07/17/1998
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