Clearance Summary
Aurora received FDA 510(k) clearance under submission number K251153, sponsored by Ge Medical Systems Israel. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-06-12.
- Submission: K251153
- Applicant / Sponsor: Ge Medical Systems Israel
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1200
- Decision date: 2025-06-12
Classification & Regulation
This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.