FDA 510(k) Application Details - K051079

Device Classification Name	Accessories, Pump, Infusion   More FDA Info for this Device
510(K) Number	K051079
Device Name	Accessories, Pump, Infusion
Applicant	HOSPICARE, INC. 275 NORTH FIELD DRIVE DEPT. 389, BLDG. H2 LAKE FOREST, IL 60045 US Other 510(k) Applications for this Company
Contact	Yuliya Matlin Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	MRZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/27/2005
Decision Date	05/19/2005
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