FDA 510(k) Application Details - K023548

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K023548
Device Name	Catheter, Percutaneous
Applicant	VELOCIMED 11400 73RD AVENUE NORTH SUITE 134 MAPLE GROVE, MN 55369 US Other 510(k) Applications for this Company
Contact	JOHN CARLINE 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	10/22/2002
Decision Date	08/04/2003
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