K242951
- 510(k) number
- K242951
- Device name
- Diode laser hair removal machine (QDTM-02)
- Applicant
- Beijing Nubway S&T Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-04-28
- Date received
- 2024-09-25
- 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: K242951.pdf
Official FDA record: K242951
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.