Clearance Summary
ScandiDos Delta4 Phantom+ received FDA 510(k) clearance under submission number K151180, sponsored by Scandidos AB. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2015-08-19.
- Submission: K151180
- Applicant / Sponsor: Scandidos AB
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 2015-08-19
Classification & Regulation
This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.