Dilon Technologies, Inc.
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) | K110384 | DILON 6800 ACELLA (ACELLA) | IYX | 2011-05-03 | View |
| 510(k) | K984466 | DILON 2000, MODEL 2000-6X8 AND DILON 2000, MODEL 2000-5X5 | IYX | 1999-03-16 | View |
No matching devices.
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