Clearance Summary
Dolphin/IQ and Dolphin/4D received FDA 510(k) clearance under submission number K170859, sponsored by Viasonix , 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 2017-11-14.
- Submission: K170859
- Applicant / Sponsor: Viasonix , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1550
- Decision date: 2017-11-14
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.