K250762
- 510(k) number
- K250762
- Device name
- ULTRASONIC PROBE UM-S20-17S (UM-S20-17S); ULTRASONIC PROBE UM-S20-20R (UM-S20-20R)
- Applicant
- Olympus Medical Systems Corporation JP
- Product code
- ITX — Transducer, Ultrasonic, Diagnostic
- Decision date
- 2025-07-11
- Date received
- 2025-03-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250762.pdf
Official FDA record: K250762
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.