K240747
- 510(k) number
- K240747
- Device name
- Medical Diode Laser (M2-GK)
- Applicant
- Wuhan Pioon Technology Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-06-17
- Date received
- 2024-03-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.9 MB · U.S. public domain
Also available from FDA: K240747.pdf
Official FDA record: K240747
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.