K233473
- 510(k) number
- K233473
- Device name
- DEKA LOTUS
- Applicant
- El.En S.P.A. IT
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2024-05-16
- Date received
- 2023-10-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K233473.pdf
Official FDA record: K233473
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.