K243123
- 510(k) number
- K243123
- Device name
- IPL Treatment Device (MDSQMC-01)
- Applicant
- Medusa (Guangxi)Medical Devices Co., Ltd. CN
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2025-07-03
- Date received
- 2024-09-30
- 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: K243123.pdf
Official FDA record: K243123
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.