K252236
- 510(k) number
- K252236
- Device name
- CP Relief Wand Rx - TENS/NMES
- Applicant
- N & C Holdings, LLC MO · US
- Product code
- GZJ — Stimulator, Nerve, Transcutaneous, For Pain Relief
- Decision date
- 2025-08-15
- Date received
- 2025-07-17
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K252236.pdf
Official FDA record: K252236
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.