Class Class II
CP Relief Wand Rx – TENS/NMES (K252236)
Description
CP Relief Wand Rx - TENS/NMES by N & C Holdings, LLC, an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK252236
Clearance Date2025-08-15
Clearance TypeSpecial
Product CodeGZJ
Regulation Number882.5890
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K252236
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. CP Relief Wand Rx – TENS/NMES (K252236) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232441 | Unipro (K-UNIPRO-US) | Tenscare, Ltd. | 2024 |
| K133779 | CP RELIEF WAND | Mid-America Medical Innovations, LLC | 2014 |
Trace the full predicate network for K252236
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.