ClearanceBrief
Company ยท JP

Fujifilm Corporaton

FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2023. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GCJLaparoscope, General & Plastic Surgery2
EOQBronchoscope (Flexible Or Rigid)1
FDAEnteroscope And Accessories1
FDSGastroscope And Accessories, Flexible/Rigid1
LLZSystem, Image Processing, Radiological1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 27, 2023K221551FUJIFILM Endoscope Model EI-740D/S
Fujifilm Corporaton, JP
FDS
Jan 11, 2023K223295Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500D
Fujifilm Corporaton, JP
FDA
Nov 10, 2022K220957FUJIFILM Endoscope Model EB-710P
Fujifilm Corporaton, JP
EOQ
Dec 2, 2021K212950FUJIFILM Video Laparoscope EL-R740M30
Fujifilm Corporaton, JP
GCJ
Jun 30, 2021K203717Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0
Fujifilm Corporaton, JP
GCJ
Aug 27, 2020K200973Synapse 3D Cardiac Tools
Fujifilm Corporaton, JP
LLZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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