K261841
- 510(k) number
- K261841
- Device name
- Q Switched Nd:YAG Laser machine (QLQW-01)
- Applicant
- Beijing Nubway S&T Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2026-08-11
- Date received
- 2026-06-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K261841.pdf
Official FDA record: K261841
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.