K233760
- 510(k) number
- K233760
- Device name
- Mjolnir Pro. (Multielectrode plasma)
- Applicant
- Shenzhen Leaflife Technology Co., Ltd. CN
- Product code
- QVJ — Low Power Electrosurgical Devices For Skin Lesion De
- Decision date
- 2024-02-20
- Date received
- 2023-11-24
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233760.pdf
Official FDA record: K233760
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.