Exonix Research Corp.
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) | K923681 | EXONOX PERCUTANEOUS INTRODUCER SYSTEM W/ HEMOSTASI | DYB | 1993-01-21 | View |
| 510(k) | K915136 | ATRAUMATIC TIP ANGIOGRAPHIC CATHETER | DQO | 1992-01-27 | View |
No matching devices.
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