Clearance Summary
LASER SYSTEM YELLOWSTAR received FDA 510(k) clearance under submission number K013940, sponsored by Asclepion-Meditec AG. 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 2002-02-26.
- Submission: K013940
- Applicant / Sponsor: Asclepion-Meditec AG
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2002-02-26
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.