K233470
- 510(k) number
- K233470
- Device name
- DEKA LILY
- Applicant
- El.En S.P.A. IT
- Product code
- NGX — Stimulator, Muscle, Powered, For Muscle Conditioning
- Decision date
- 2023-12-19
- Date received
- 2023-10-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
510(k) Summary (official FDA PDF): K233470.pdf
Official FDA record: K233470
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.