Fujifilm Corporaton

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221551FUJIFILM Endoscope Model EI-740D/SJanuary 27, 2023
K223295Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500DJanuary 11, 2023
K220957FUJIFILM Endoscope Model EB-710PNovember 10, 2022
K212950FUJIFILM Video Laparoscope EL-R740M30December 2, 2021
K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0June 30, 2021
K200973Synapse 3D Cardiac ToolsAugust 27, 2020