Fujifilm Corporaton
Fujifilm Corporaton appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 27, 2023.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K221551 | FUJIFILM Endoscope Model EI-740D/S | January 27, 2023 |
| K223295 | Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D | January 11, 2023 |
| K220957 | FUJIFILM Endoscope Model EB-710P | November 10, 2022 |
| K212950 | FUJIFILM Video Laparoscope EL-R740M30 | December 2, 2021 |
| K203717 | Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 | June 30, 2021 |
| K200973 | Synapse 3D Cardiac Tools | August 27, 2020 |