FDA 510(k) Application Details - K023083

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K023083
Device Name	Pump, Infusion
Applicant	METTLER ELECTRONICS CORP. 1333 SOUTH CLAUDINA ST. ANAHEIM, CA 92805 US Other 510(k) Applications for this Company
Contact	ROBERT E FLEMING 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	09/17/2002
Decision Date	02/28/2003
Decision	ST - Substantially Equivalent - Subject to Tracking Reg.
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review