Orion Corporation Soredex
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K983267 | DIGORA FOR WINDOWS 2.0 | MUH | 1998-12-30 | View |
| 510(k) | K974877 | CRANEX TOME CEPH, OR CRANEX TOME | EHD | 1998-03-27 | View |
| 510(k) | K934949 | DIGORA | IXK | 1994-02-10 | View |
| 510(k) | K880982 | ORALIX PAN DC III CEPH OR PANORAMIC MODE ONLY | KPR | 1988-06-06 | View |
No matching devices.
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