FDA 510(k) Applications Submitted by KEVIN DRISKO

FDA 510(k) Number Submission Date Device Name Applicant
K060487 02/24/2006 LIFESTENT FLEXSTAR XL BILIARY STENT SYSTEM EDWARDS LIFESCIENCES, LLC.
K030630 02/27/2003 EDWARDS DIRECTIONAL CATHETER EDWARDS LIFESCIENCES, LLC.
K050627 03/11/2005 LIFESTENT TURBO BILIARY STENT SYSTEMS EDWARDS LIFESCIENCES, LLC.
K061235 05/03/2006 LIFESTENT TURBO BILIARY STENT SYSTEM EDWARDS LIFESCIENCES, LLC.
K022026 06/21/2002 MEDTRONIC AVE BRIDGE POLARIS BILIARY STENT SYSTEM (POLARIS) MEDTRONIC AVE, INC.
K052132 08/05/2005 MODIFICATION TO: LIFESTENT VALEO BILIARY STENT SYSTEM EDWARDS LIFESCIENCES, LLC.
K052149 08/08/2005 EDWARDS PERIPHERAL DILATION CATHETER EDWARDS LIFESCIENCES, LLC.
K032587 08/22/2003 EDWARDS PERIPHERAL DILATATION CATHETER EDWARDS LIFESCIENCES, LLC.
K042985 10/29/2004 LIFESTENT NT35 BILIARY STENT SYSTEM EDWARDS LIFESCIENCES, LLC.
K053404 12/07/2005 LIFESTENT FLEXSTART BILIARY STENT SYSTEM EDWARDS LIFESCIENCES, LLC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact