FDA 510(k) Application Details - K070380

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K070380
Device Name	Clamp, Vascular
Applicant	CARDIO LIFE RESEARCH, S.A. 220 RIVER ROAD CLAREMONT, NH 03743 US Other 510(k) Applications for this Company
Contact	WILLIAM GREENROSE 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	02/08/2007
Decision Date	06/08/2007
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