K233090
- 510(k) number
- K233090
- Device name
- DEKA AGAIN PRO family
- Applicant
- El.En S.P.A. IT
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2023-10-27
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K233090.pdf
Official FDA record: K233090
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.