K250341
- 510(k) number
- K250341
- Device name
- Sensilift Pro (ST300XXYYZZZ)
- Applicant
- El Global Trade, Ltd. IL
- Product code
- PAY — Over-The-Counter Radiofrequency Coagulation Device F
- Decision date
- 2026-01-06
- Date received
- 2025-02-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K250341.pdf
Official FDA record: K250341
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.