FDA 510(k) Application Details - K101677

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K101677
Device Name	Set, Administration, Intravascular
Applicant	HOSPIRA, INC. 375 N FIELD DRIVE LAKE FOREST, IL 60045 US Other 510(k) Applications for this Company
Contact	KAREN KEENER 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	06/15/2010
Decision Date	08/11/2010
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