Clearance Summary
Digital Radiographic Imaging Acquisition Software - DR (RiasDR) received FDA 510(k) clearance under submission number K251038, sponsored by Shen Zhen Cambridge-Hit Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-08-06.
- Submission: K251038
- Applicant / Sponsor: Shen Zhen Cambridge-Hit Co., Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.2050
- Decision date: 2025-08-06
Classification & Regulation
This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.