FDA 510(k) Application Details - K031419

Device Classification Name	Container, I.V.   More FDA Info for this Device
510(K) Number	K031419
Device Name	Container, I.V.
Applicant	LABORATORIOS GRIFOLS, S.A. POL. LEVANTE C/CAN GUASCH, 2 PARETS DEL VALLES, BARCELONA 08150 ES Other 510(k) Applications for this Company
Contact	SEBASTIAN GASCON 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	05/05/2003
Decision Date	11/24/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review