Clearance Summary
E1000 Dx Digital Pathology Solution received FDA 510(k) clearance under submission number K241717, sponsored by Shandon Diagnostics Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Pathology review panel. The statutory decision date of record is 2025-02-28.
- Submission: K241717
- Applicant / Sponsor: Shandon Diagnostics Limited
- Clearance pathway: Traditional
- Review panel: Pathology
- Device class: Class II
- Regulation citation: 21 CFR 864.3700
- Decision date: 2025-02-28
Classification & Regulation
This clearance is catalogued under FDA product code PSY and 21 CFR 864.3700, within the Pathology review panel as a Class II device.