# K252236: CP Relief Wand Rx - TENS/NMES

- Pathway: 510(k) (Special)
- Applicant: N & C Holdings, LLC
- Decided: Aug 15, 2025 after 29 days
- Product code: GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K010782 (2001). 29 ancestors in all.
No later device cites it as a predicate yet.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133779: CP Relief Wand, Mid-America Medical Innovations, LLC (2014) Summary page 5.
- K232441: Unipro (K-UNIPRO-US), Tenscare, Ltd. (2024) Summary page 5.

## Indications for use
As a TENS device, the CP Relief Wand Rx - TENS/NM ES is intended for use as an adjunctive therapy for pain management for medical purposes such as symptomatic relief of chronic intractable pain and relief of acute post surgical and post-traumatic pain. As an EMS device, the CP Relief Wand Rx - TENS/NM ES is intended for use for relaxation of muscle spasm, increasing local blood circulation, muscle re-education, prevention or retardation of disuse atrophy, prevention of venous thrombosis of the calf muscles immediately after surgery, and maintaining on increasing range of motion.

Source page: https://510kreport.com/device/K252236
Methodology: https://510kreport.com/methodology