FDA 510(k) Application Details - K160866

Device Classification Name	Filter, Intravascular, Cardiovascular   More FDA Info for this Device
510(K) Number	K160866
Device Name	Filter, Intravascular, Cardiovascular
Applicant	C.R. BARD, INC. 1625 W. THIRD ST. TEMPE, AZ 85281 US Other 510(k) Applications for this Company
Contact	LAURIE SANG 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	03/30/2016
Decision Date	04/29/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review