K240676
- 510(k) number
- K240676
- Device name
- ULTIMUS Series Ultrasound Diagnostic System
- Applicant
- Vinno Technology (Suzhou) Co.,Ltd CN
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2024-12-16
- Date received
- 2024-03-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K240676.pdf
Official FDA record: K240676
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.