K232885
- 510(k) number
- K232885
- Device name
- Dawn Diode Laser System
- Applicant
- Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd CN
- Product code
- NVK — Laser, Dental, Soft Tissue
- Decision date
- 2024-02-28
- Date received
- 2023-09-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232885.pdf
Official FDA record: K232885
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.