K241860
- 510(k) number
- K241860
- Device name
- Diode Laser Hair Removal System
- Applicant
- Beijing Winkonlaser Technology Limited CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-09-25
- Date received
- 2024-06-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K241860.pdf
Official FDA record: K241860
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.