Clearance Summary
D-Laser Blue, D-Laser 16 received FDA 510(k) clearance under submission number K210367, sponsored by Guilin Woodpecker Medical Instrument Co., Ltd.. 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 2022-03-10.
- Submission: K210367
- Applicant / Sponsor: Guilin Woodpecker Medical Instrument Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2022-03-10
Classification & Regulation
This clearance is catalogued under FDA product code NVK and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.