K230459
- 510(k) number
- K230459
- Device name
- C.C. Life 21
- Applicant
- 21 Equipment S.R.L. IT
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2023-10-19
- Date received
- 2023-02-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K230459
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.