K242789
- 510(k) number
- K242789
- Device name
- Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006)
- Applicant
- Dongguan Laiguang Electronic Technology Co., Ltd. CN
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2025-01-02
- Date received
- 2024-09-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242789.pdf
Official FDA record: K242789
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.