FDA 510(k) Application Details - K030888

Device Classification Name	Container, I.V.   More FDA Info for this Device
510(K) Number	K030888
Device Name	Container, I.V.
Applicant	METRIX CO. 4400 CHAVENELLE RD. DUBUQUE, IA 52002 US Other 510(k) Applications for this Company
Contact	JAMES J OLDHAM Other 510(k) Applications for this Contact
Regulation Number	880.5025   More FDA Info for this Regulation Number
Classification Product Code	KPE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/21/2003
Decision Date	04/02/2003
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