FDA 510(k) Application Details - K021988

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K021988
Device Name	Pump, Infusion
Applicant	MEDRAD, INC. ONE MEDRAD DR. INDIANOLA, PA 15051 US Other 510(k) Applications for this Company
Contact	LORRAINE R FREDES 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	06/18/2002
Decision Date	08/29/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	Y
Expedited Review