FDA 510(k) Application Details - K091624

Device Classification Name	Catheter, Percutaneous   More FDA Info for this Device
510(K) Number	K091624
Device Name	Catheter, Percutaneous
Applicant	VIA BIOMEDICAL, INC. 6655 WEDGEWOOD RD, SUITE 150 MAPLE GROVE, MN 55311 US Other 510(k) Applications for this Company
Contact	FERNANDO DI CAPRIO 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	06/03/2009
Decision Date	10/15/2009
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