Clearance Summary
Light-Guide Cables received FDA 510(k) clearance under submission number K223183, sponsored by Olympus Winter & Ibe GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2023-01-13.
- Submission: K223183
- Applicant / Sponsor: Olympus Winter & Ibe GmbH
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4580
- Decision date: 2023-01-13
Classification & Regulation
This clearance is catalogued under FDA product code HBI and 21 CFR 878.4580, within the General, Plastic Surgery review panel as a Class II device.