K254220
- 510(k) number
- K254220
- Device name
- Reusable 3 Button Fingerswitch Wand
- Applicant
- Soniquence, LLC NY · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2026-01-27
- Date received
- 2025-12-29
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K254220.pdf
Official FDA record: K254220
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.