K232532
- 510(k) number
- K232532
- Device name
- Nd:Yag Laser Therapy Systems
- Applicant
- Beijing Unt Technology Co., Ltd. CN
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2023-11-02
- Date received
- 2023-08-21
- 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: K232532.pdf
Official FDA record: K232532
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.