FDA 510(k) Application Details - K070238

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K070238
Device Name	Catheter, Percutaneous
Applicant	AGA MEDICAL CORP. 682 MENDELSSOHN AVE. PLYMOUTH, MN 55427 US Other 510(k) Applications for this Company
Contact	DAVID D COX Other 510(k) Applications for this Contact
Regulation Number	870.1250   More FDA Info for this Regulation Number
Classification Product Code	DQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/25/2007
Decision Date	02/28/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review