K243330
- 510(k) number
- K243330
- Device name
- LYMA Laser PRO
- Applicant
- Lyma Life , Ltd. GB
- Product code
- OHS — Light Based Over The Counter Wrinkle Reduction
- Decision date
- 2025-02-21
- Date received
- 2024-10-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K243330.pdf
Official FDA record: K243330
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.