FDA 510(k) Application Details - K014091

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K014091
Device Name	Pump, Infusion
Applicant	STRYKER CORP. 4100 E. MILHAM AVE. KALAMAZOO, MI 49001 US Other 510(k) Applications for this Company
Contact	NICOLE PETTY 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	12/12/2001
Decision Date	12/31/2001
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