FDA 510(k) Application Details - K121634

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K121634
Device Name	Set, Administration, Intravascular
Applicant	BAXTER HEALTHCARE CORPORATION 25212 W. ILLINOIS ROUTE 120 ROUND LAKE, IL 60073 US Other 510(k) Applications for this Company
Contact	NANETTE HEDDEN Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/04/2012
Decision Date	06/29/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review