FDA 510(k) Application Details - K020251

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K020251
Device Name	Pump, Infusion
Applicant	I-FLOW CORP. 20202 WINDROW DR. LAKE FOREST, CA 92630 US Other 510(k) Applications for this Company
Contact	SHANE NOEHRE 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	01/24/2002
Decision Date	02/15/2002
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