# K131910: MPP

- Pathway: 510(k) (Traditional)
- Applicant: Marc Pro
- Decided: Jan 24, 2014 after 212 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: 5 generations back to K940301 (1994). 13 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081998: H-Wave Sport, Electronic Waveform Laboratory, Inc. (2009) Summary page 1.
- K121757: Healthmateforever, Healthmate International, LLC (2012) Summary page 1.
- K112485: H-WAVE, Electronic Waveform Lab, Inc. (2011) Summary page 1.

## Most influential descendants
- K160255: HBOTC Muscle and Nerve Stimulator (2016), 0 descendants of its own

## Indications for use
The MPP is to be used for temporary relief of pain associated with sore and aching muscles in the shoulder, waist, back, neck, upper extremities (arm), and lower extremities (leg) due to strain from exercise and normal household and work activities. The MPP is intended for muscle conditioning by stimulating muscle in order to improve or facilitate muscle performance.

Source page: https://510kreport.com/device/K131910
Methodology: https://510kreport.com/methodology