# K183110: LIVIA

- Pathway: 510(k) (Traditional)
- Applicant: Lifecare, Ltd.
- Decided: May 4, 2020 after 543 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: 3 generations back to K130802 (2013). 3 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163153: Livia, Lifecare, Ltd. (2017) Summary page 4.

## Most influential descendants
- K233054: Well-Life Pain Relief (Menstrual Plus) Electrical Stimulator; TENS/EMS WITH Menstrual Relief Stimulator; Well-Life Pain Relief Stimulator; Menstrual Plus Stimulator (2024), 0 descendants of its own
- K230926: Ova+ (K-OVAP-USA) (2023), 0 descendants of its own
- K220997: Wireless TENS/EMS, Bruno, Aela (2022), 0 descendants of its own

## Indications for use
The Livia is designed for symptomatic relief and management of chronic pain, and 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. The Livia is also indicated for temporary relief of pain associated with dysmenorrhea (menstrual cramps) when used with over-the-counter pain medication.

Source page: https://510kreport.com/device/K183110
Methodology: https://510kreport.com/methodology