K243929
- 510(k) number
- K243929
- Device name
- Oligio X
- Applicant
- Wontech Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-01-21
- Date received
- 2024-12-20
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K243929.pdf
Official FDA record: K243929
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.