Clearance Summary
Advanced Intelligent Volumetric Ultrasound System, Model AiVUS 1000 received FDA 510(k) clearance under submission number K190314, sponsored by Mednovel Technology, Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2019-10-09.
- Submission: K190314
- Applicant / Sponsor: Mednovel Technology, Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2019-10-09
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.