K232001
- 510(k) number
- K232001
- Device name
- Nu Skin RenuSpa iO
- Applicant
- Nse Products, Inc. UT · US
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2023-11-21
- Date received
- 2023-07-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K232001.pdf
Official FDA record: K232001
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.