FDA 510(k) Applications Submitted by ENDOTHELIX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072919 | 10/15/2007 | VENDYS, MODEL 6000 B B/C | ENDOTHELIX, INC. |
| K060980 | 04/10/2006 | VENDYS MODEL 5000 B/BC | ENDOTHELIX, INC. |
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