FDA 510(k) Applications Submitted by BYPASS LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K020470 | 02/12/2002 | MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE | BYPASS LTD. |
| K011589 | 05/23/2001 | CORLINK AAD (3.5 TO 6.0 M M OUTER DIAMETER VESSELS),MODEL 200-064, CORLINK AAD (2.0 TO 4.0 MM OUTER DIAMETER VESSELS), M | BYPASS LTD. |
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