FDA 510(k) Application Details - K012083

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K012083
Device Name	Catheter, Percutaneous
Applicant	MEDTRONIC VASCULAR 7000 CENTRAL AVE. N.E. MINNEAPOLIS, MN 55432 US Other 510(k) Applications for this Company
Contact	KAREN REIDT 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	07/03/2001
Decision Date	08/28/2001
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	N
Expedited Review