K233401
- 510(k) number
- K233401
- Device name
- Portable Liver Elastography Ultrasound Diagnostic System (Liverscan Mobile)
- Applicant
- Eieling Technology Limited CN
- Product code
- IYO — System, Imaging, Pulsed Echo, Ultrasonic
- Decision date
- 2024-02-12
- Date received
- 2023-10-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Radiology
510(k) Summary (official FDA PDF): K233401.pdf
Official FDA record: K233401
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.