K240857
- 510(k) number
- K240857
- Device name
- Youmagic FLM System (YM5-U1)
- Applicant
- We Medical Technology (Wuxi) Co., Ltd. CN
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-05-15
- Date received
- 2024-03-28
- 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: K240857.pdf
Official FDA record: K240857
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.