Clearance Summary
RadiForce RX670; RadiForce RX670-AR received FDA 510(k) clearance under submission number K241441, sponsored by Eizo Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-07-16.
- Submission: K241441
- Applicant / Sponsor: Eizo Corporation
- Clearance pathway: Abbreviated
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2024-07-16
Classification & Regulation
This clearance is catalogued under FDA product code PGY and 21 CFR 892.2050, within the Radiology review panel as a Class II device.