FDA 510(k) Application Details - K073090

Device Classification Name	Filter, Intravascular, Cardiovascular   More FDA Info for this Device
510(K) Number	K073090
Device Name	Filter, Intravascular, Cardiovascular
Applicant	C.R. BARD, INC. PO BOX 1740 1625 WEST 3RD STREET TEMPE, AZ 85281-1740 US Other 510(k) Applications for this Company
Contact	GENEVIEVE BALUTOWSKI Other 510(k) Applications for this Contact
Regulation Number	870.3375   More FDA Info for this Regulation Number
Classification Product Code	DTK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/01/2007
Decision Date	01/15/2008
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