510(k) K240142

Device
FUJIFILM Endoscope Model EG-840N; FUJIFILM Endoscope Model EG-840T; FUJIFILM Endoscope Model EG-840TP
Applicant
Fujifilm Corporation
510(k) number
K240142
Product code
FDS
Decision
Substantially Equivalent (SESE)
Decision date
2024-09-04
Date received
2024-01-18
Regulation
876.1500
Classification name
Gastroscope And Accessories, Flexible/Rigid
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Chaitrali Kulkarni
Address
798 Miyanodai Kaisei-Machi Ashigara Kami-Gun JP 258-8538 258-8538

FDA Registration Numbers

Source Documents

510(k) summary PDF

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