K251049
- 510(k) number
- K251049
- Device name
- SurgiLight 1470 Diode Laser System (Model:Halo)
- Applicant
- Micro-Energy Medical Technology Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-07-02
- Date received
- 2025-04-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K251049.pdf
Official FDA record: K251049
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.