Clearance Summary
LumenEye® X1 endoscope (LX1-SCP-203); LumenEye® X1 consumables (LX1-CSB-201); LumenEye® X1 Consumable Carton (25 Sets) (LX1-CSP-201 ) received FDA 510(k) clearance under submission number K232262, sponsored by Surgease Innovations Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2023-11-30.
- Submission: K232262
- Applicant / Sponsor: Surgease Innovations Limited
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2023-11-30
Classification & Regulation
This clearance is catalogued under FDA product code FAN and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.