K243764
- 510(k) number
- K243764
- Device name
- Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)
- Applicant
- Wuhan Pioon Technology Co., Ltd. CN
- Product code
- NVK — Laser, Dental, Soft Tissue
- Decision date
- 2025-05-08
- Date received
- 2024-12-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K243764.pdf
Official FDA record: K243764
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.