# K223151: Nu-beca Transcutaneous Electrical Nerve Stimulation

- Pathway: 510(k) (Traditional)
- Applicant: Nu-Beca & Maxcellent Co.
- Decided: Jul 19, 2023 after 287 days
- Product code: NUH (Stimulator, Nerve, Transcutaneous, Over-The-Counter)
- 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 K912178 (1991). 16 ancestors in all.
No later device cites it as a predicate yet.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211403: HIVOX OTC Electrical Stimulator, FT610-B, Hivox Biotek, Inc. (2021) Summary page 4.

## Indications for use
The nu-beca Transcutaneous Electrical Nerve Stimulation is indicated for temporary relief of pain associated with sore and aching muscles in the lower back and upper and lower extremities (arm and/or leg) due to strain from exercise or normal household and work activities.

Source page: https://510kreport.com/device/K223151
Methodology: https://510kreport.com/methodology