# K151035: PulseRelief

- Pathway: 510(k) (Traditional)
- Applicant: Philips Consumer Lifestyle
- Decided: Jul 21, 2015 after 95 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: 1 generation back to K130802 (2013). 1 ancestor in all.
20 later devices descend from it; 7 cite it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130802: Otc Electrical Stimulator (MT9001), Otc Tens Device (LT3060), Shenzhen Dongdixin Technology Co., Ltd. (2013) Summary page 4.

## Most influential descendants
- K172079: Avail (2017), 5 descendants of its own
- K163153: Livia (2017), 4 descendants of its own
- K183110: LIVIA (2020), 3 descendants of its own
- K162479: Smart Pain Reliever, Model LT5019 (2017), 3 descendants of its own
- K173462: Wireless Pain Relieve Device Model: LT5018C (2017), 2 descendants of its own

## Indications for use
The OTC TENS/EMS stimulator PulseRelief is designed 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 or normal household work activities. It should be applied to normal, healthy, dry and clean skin of adult patients, and is to be used for stimulate healthy muscles in order to improve and facilitate muscle performance.

Source page: https://510kreport.com/device/K151035
Methodology: https://510kreport.com/methodology