Last synced on 12 October 2025 at 8:21 pm

FUJIFILM Endoscope Model EC-860P/M; FUJIFILM Endoscope Model EC-860P/L; FUJIFILM Endoscope Model EC-860S/L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243261
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/23/2025
Days to Decision
220 days
Submission Type
Summary

FUJIFILM Endoscope Model EC-860P/M; FUJIFILM Endoscope Model EC-860P/L; FUJIFILM Endoscope Model EC-860S/L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K243261
510(k) Type
Traditional
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/23/2025
Days to Decision
220 days
Submission Type
Summary