K241642
- 510(k) number
- K241642
- Device name
- Diode Laser Hair Removal System (MBT-Diode Laser)
- Applicant
- Beijing Mega Beauty Technology Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-08-02
- Date received
- 2024-06-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.7 MB · U.S. public domain
Also available from FDA: K241642.pdf
Official FDA record: K241642
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.