K251919
- 510(k) number
- K251919
- Device name
- Thulium Laser System (Deluxlase)
- Applicant
- Nanjing Bestview Laser S&T Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-09-26
- Date received
- 2025-06-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K251919.pdf
Official FDA record: K251919
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.