K244048
- 510(k) number
- K244048
- Device name
- Medi Lift Mask
- Applicant
- Ya-Man, Ltd. JP
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2025-01-16
- Date received
- 2024-12-31
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K244048.pdf
Official FDA record: K244048
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.