Known Identifiers & Locations
FEI Numbers
3001874253
Owner Operator Numbers
N/A
Locations Covered
N/A
Registered Establishments (0)
No device registration and listing records found for this entity.
510(k) Premarket Notifications (0)
No 510(k) notifications found for this entity.
FDA Recall History (1)
| Recall # |
Product Description |
Initiation Date |
Status |
Action |
| Z-0014-2009 |
Mobetron Model 1000, mobile electron linear accelerator, a device system which delivers radiation to an intraoperative site.
Reason: Docking screw/nut failure, which may result in a treatment head dropping, potentially impacting the patient.
|
2008-06-20 |
Terminated
|
View Details
|
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