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. |
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