K233862
- 510(k) number
- K233862
- Device name
- NUNA LUX (NUNL528)
- Applicant
- Premier North America, Inc. FL · US
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2024-03-01
- Date received
- 2023-12-06
- 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: K233862.pdf
Official FDA record: K233862
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.