Clearance Summary
GME LinScan Lite 808 Laser System received FDA 510(k) clearance under submission number K180518, sponsored by Gme German Medical Engineering 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 2018-07-23.
- Submission: K180518
- Applicant / Sponsor: Gme German Medical Engineering GmbH
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2018-07-23
Classification & Regulation
This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.