Nordion International, 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) | K963497 | GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0 | MOT | 1996-11-08 | View |
| 510(k) | K952291 | GAMMACELL 3000 ELAN | MOT | 1995-08-25 | View |
No matching devices.
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