FDA 510(k) Application Details - K052052

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K052052
Device Name	Pump, Infusion
Applicant	HOSPIRA, INC. 275 N. FIELD DR., BLDG. H-2 D-389 LAKE FOREST, IL 60045-5045 US Other 510(k) Applications for this Company
Contact	PATRICIA MELERSKI Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	FRN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/29/2005
Decision Date	08/24/2005
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