Mitsubishi Heavy Industries, Ltd.
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) | K122450 | MHI-TM2000 LINEAR ACCELERATOR SYSTEM VERO IMAVIS | IYE | 2012-10-03 | View |
| 510(k) | K072047 | MHI-TM2000 LINEAR ACCELERATOR SYSTEM | IYE | 2007-08-29 | View |
No matching devices.
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