Bypass , Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K020470 | MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE | FZP | 2002-03-08 | View |
| 510(k) | K011589 | 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 | NCA | 2001-12-26 | View |
No matching devices.
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