FDA 510(k) Application Details - K021480

Device Classification Name	Set, Administration, Intravascular   More FDA Info for this Device
510(K) Number	K021480
Device Name	Set, Administration, Intravascular
Applicant	CODAN US CORP. 3511 WEST SUNFLOWER AVE. SANTA ANA, CA 92704-6944 US Other 510(k) Applications for this Company
Contact	MARILYN R POURAZAR Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	FPA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/08/2002
Decision Date	06/27/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review