FDA 510(k) Application Details - K080695

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K080695
Device Name	Set, Administration, Intravascular
Applicant	NORTHWIND TECHNOLOGIES, CORP. 20171 BOWENS RD. MANCHESTER, MI 48158 US Other 510(k) Applications for this Company
Contact	DAWN I MOORE Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/11/2008
Decision Date	07/01/2008
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review