FDA 510(k) Application Details - K024239

Device Classification Name	Set, I.V. Fluid Transfer   More FDA Info for this Device
510(K) Number	K024239
Device Name	Set, I.V. Fluid Transfer
Applicant	ABBOTT LABORATORIES DEPT 0389 BLDG J-45 200 ABBOTT PARK ROAD ABBOTT PARK, IL 60064-6133 US Other 510(k) Applications for this Company
Contact	NICOHL R WILDING Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	LHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/23/2002
Decision Date	01/13/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review