K232033
- 510(k) number
- K232033
- Device name
- HYBRIDknife® flex
- Applicant
- Erbe Elektromedizin GmbH DE
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2023-11-29
- Date received
- 2023-07-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232033.pdf
Official FDA record: K232033
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.