Clearance Summary
CLL- V1 LIGHT SOURCE received FDA 510(k) clearance under submission number K130819, sponsored by Olympus Winter & Ibe GmbH. 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 2013-06-19.
- Submission: K130819
- Applicant / Sponsor: Olympus Winter & Ibe GmbH
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.1500
- Decision date: 2013-06-19
Classification & Regulation
This clearance is catalogued under FDA product code NTN and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.