First Source, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2024-07-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240009 | iQFlex Pro | IZL | 2024-07-03 | View |
| 510(k) | K221081 | iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System | IZL | 2022-06-13 | View |
| 510(k) | K203703 | I-Q View | MQB | 2021-03-24 | View |
No matching devices.