Clearance Summary
Clarius Ultrasound System received FDA 510(k) clearance under submission number K163138, sponsored by Clarius Mobile Health Corp.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-11-30.
- Submission: K163138
- Applicant / Sponsor: Clarius Mobile Health Corp.
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2016-11-30
Classification & Regulation
This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.