K233120
- 510(k) number
- K233120
- Device name
- CWM-930S, FIXER DV9
- Applicant
- Chungwoo Co., Ltd. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-05-23
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233120.pdf
Official FDA record: K233120
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.