K220493
- 510(k) number
- K220493
- Device name
- Plaxpot Multi Plasma
- Applicant
- Gcs Co. Limited KR
- Product code
- QVJ — Low Power Electrosurgical Devices For Skin Lesion De
- Decision date
- 2023-10-27
- Date received
- 2022-02-22
- 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: K220493.pdf
Official FDA record: K220493
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.