Clearance Summary
SENTINEL received FDA 510(k) clearance under submission number K120668, sponsored by C-Rad Positioning 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 2012-07-30.
- Submission: K120668
- Applicant / Sponsor: C-Rad Positioning AB
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.5050
- Decision date: 2012-07-30
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.