Clearance Summary
Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43) received FDA 510(k) clearance under submission number K243556, sponsored by Iray Imaging Technology (Haining) Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-03-18.
- Submission: K243556
- Applicant / Sponsor: Iray Imaging Technology (Haining) Limited
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1680
- Decision date: 2025-03-18
Classification & Regulation
This clearance is catalogued under FDA product code MQB and 21 CFR 892.1680, within the Radiology review panel as a Class II device.