FDA 510(k) Applications Submitted by TIFFINI LALUDE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070548 | 02/26/2007 | C-PORT FLEXA DISTAL ANASTOMOSIS SYSTEM | CARDICA, INC. |
| K063644 | 12/07/2006 | CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM | CARDICA, INC. |
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