K233734
- 510(k) number
- K233734
- Device name
- Interson USB Ultrasound System
- Applicant
- Interson Corporation CA · US
- Product code
- IYN — System, Imaging, Pulsed Doppler, Ultrasonic
- Decision date
- 2023-12-22
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Radiology
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K233734.pdf
Official FDA record: K233734
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.