Clearance Summary
Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) received FDA 510(k) clearance under submission number K242789, sponsored by Dongguan Laiguang Electronic Technology 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 2025-01-02.
- Submission: K242789
- Applicant / Sponsor: Dongguan Laiguang Electronic Technology Co., Ltd.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4810
- Decision date: 2025-01-02
Classification & Regulation
This clearance is catalogued under FDA product code OHS and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.