Clearance Summary
SpotLight/SpotLight Duo with Low Dose Lung Cancer Screening Option received FDA 510(k) clearance under submission number K241200, sponsored by Arineta , 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 2025-01-13.
- Submission: K241200
- Applicant / Sponsor: Arineta , Ltd.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1750
- Decision date: 2025-01-13
Classification & Regulation
This clearance is catalogued under FDA product code JAK and 21 CFR 892.1750, within the Radiology review panel as a Class II device.