K232441
- 510(k) number
- K232441
- Device name
- Unipro (K-UNIPRO-US)
- Applicant
- Tenscare, Ltd. GB
- Product code
- GZJ — Stimulator, Nerve, Transcutaneous, For Pain Relief
- Decision date
- 2024-08-30
- Date received
- 2023-08-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K232441.pdf
Official FDA record: K232441
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.