Fujifilm Corporaton
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories5
Latest FDA decision2023-01-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K221551 | FUJIFILM Endoscope Model EI-740D/S | FDS | 2023-01-27 | View |
| 510(k) | K223295 | Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D | FDA | 2023-01-11 | View |
| 510(k) | K220957 | FUJIFILM Endoscope Model EB-710P | EOQ | 2022-11-10 | View |
| 510(k) | K212950 | FUJIFILM Video Laparoscope EL-R740M30 | GCJ | 2021-12-02 | View |
| 510(k) | K203717 | Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 | GCJ | 2021-06-30 | View |
| 510(k) | K200973 | Synapse 3D Cardiac Tools | LLZ | 2020-08-27 | View |
No matching devices.