Last synced on 25 January 2026 at 3:41 am

Endoscope Model EI-740D/S

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210162
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/9/2021
Days to Decision
78 days
Submission Type
Summary

Endoscope Model EI-740D/S

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210162
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/9/2021
Days to Decision
78 days
Submission Type
Summary