FDA 510(k) Applications Submitted by JOANNA KUSKOWSKI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040667 |
03/15/2004 |
XPERT BILIARY STENT, MODELS EX8L6006, EX8L3008, EX8L4008, EX8L6008, EX8S6006, EX8S3008, EX8S4008, EX8S6008 |
ABBOTT LABORATORIES |
| K040954 |
04/13/2004 |
FOX PLUS PTA CATHETER |
ABBOTT LABORATORIES INC |
| K031331 |
04/28/2003 |
WZ SELF-EXPANDING STENT TRANSHEPATIC BILIARY SYSTEM |
ABBOTT VASCULAR INC. |
| K041962 |
07/21/2004 |
XPAND BALLOON-EXPANDABLE TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 20587, 20588, 20589, 20603, 20604, 20605 |
ABBOTT LABORATORIES |
| K032929 |
09/22/2003 |
MODIFICATION TO:XCEED NITINOL SELF-EXPANDING TRANSHEPATIC BILIARY STENT SYSTEM, MODELS 14819, 14820, 14821, 14822, 14822 |
ABBOTT VASCULAR INC. |
| K033537 |
11/10/2003 |
SELFX XPERT BILIARY STENT, MODELS EX8L2005, EX8L3005, EX8L4005, EX8L2006, EX8L3006, EX8L4006, EX8S2005, AND EX8S3005 |
ABBOTT LABORATORIES |
| K033909 |
12/17/2003 |
WAVEMAX BALLOON-EXPANDABLE TRANSHEPATIC BILIARY STENT SYSTEM |
ABBOTT LABORATORIES |
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