K241102
- 510(k) number
- K241102
- Device name
- Luna 4 plus
- Applicant
- Foreo, Inc. NV · US
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2024-08-20
- Date received
- 2024-04-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K241102.pdf
Official FDA record: K241102
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.