FDA 510(k) Application Details - K984060

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K984060
Device Name	Set, Administration, Intravascular
Applicant	BAXTER HEALTHCARE CORP. CLINTEC NUTRITION CO. ROUTE 120 AND WILSON ROAD ROUND LAKE, IL 60073 US Other 510(k) Applications for this Company
Contact	MARY ELLEN SNYDER 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	11/13/1998
Decision Date	07/26/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review