Digimed Corporation
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) | K103600 | PORTABLE X-RAY SYSTEM | EHD | 2011-04-08 | View |
| 510(k) | K082167 | PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX | EHD | 2008-09-26 | View |
No matching devices.
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