FDA 510(k) Application Details - K051817

Device Classification Name	Clamp, Vascular   More FDA Info for this Device
510(K) Number	K051817
Device Name	Clamp, Vascular
Applicant	CARDIVA MEDICAL, INC. P.O. BOX 10925 PLEASANTON, CA 94588 US Other 510(k) Applications for this Company
Contact	KARIN GASTINEAU 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	07/05/2005
Decision Date	12/06/2006
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