FDA 510(k) Application Details - K092503

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K092503
Device Name	Clamp, Vascular
Applicant	ADVANCED VASCULAR DYNAMICS 1910 NW 23RD PLACE PORTLAND, OR 97210 US Other 510(k) Applications for this Company
Contact	MATTHEW SEMLER Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	DXC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/14/2009
Decision Date	11/19/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review