K252211
- 510(k) number
- K252211
- Device name
- Duoblade Plus SE (DB1EP, DB1EP-T, DB1EP-H, DB1EP-TH); Duoblade Prime (DB1P, DB1P-T, DB1P-H, DB1P-TH)
- Applicant
- Cnc Technologies KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-08-11
- Date received
- 2025-07-15
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K252211.pdf
Official FDA record: K252211
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.