FDA 510(k) Applications Submitted by GUIDANT ENDOVASCULAR SOLUTIONS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060817 | 03/27/2006 | OMNILINK. 018 BILIARY STENT SYSTEM | GUIDANT ENDOVASCULAR SOLUTIONS, INC. |
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