K250701
- 510(k) number
- K250701
- Device name
- Evis Exera III Duodenovideoscope Olympus TJF-Q190V (TJF-Q190V)
- Applicant
- Olympus Medical Systems Corp. JP
- Product code
- FDT — Duodenoscope And Accessories, Flexible/Rigid
- Decision date
- 2025-06-05
- Date received
- 2025-03-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Gastroenterology, Urology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K250701.pdf
Official FDA record: K250701
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.