Clearance Summary
K3900 Ultrasound Imaging System received FDA 510(k) clearance under submission number K230511, sponsored by Maui Imaging. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-10-25.
- Submission: K230511
- Applicant / Sponsor: Maui Imaging
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2023-10-25
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.