K250361
- 510(k) number
- K250361
- Device name
- SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1
- Applicant
- Geske Beauty Tech GmbH DE
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2025-05-23
- Date received
- 2025-02-10
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K250361.pdf
Official FDA record: K250361
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.