# K102375: LUCIA

- Pathway: 510(k) (Traditional)
- Applicant: Meridian Co., Ltd.
- Decided: Feb 25, 2011 after 189 days
- Product code: ILY (Lamp, Infrared, Therapeutic Heating)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K033923 (2004). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K081962: Lapex BCS, Meridian Co., Ltd. (2008) Summary page 1.

## Most influential descendants
- K110342: Yolo Curve (2011), 0 descendants of its own

## Indications for use
The Lucia is intended to emit energy in the visible and infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of minor muscle and joint pain and stiffness, minor arthritis pain, or muscle spasm; the temporary increase in local blood circulation; and/or the temporary relaxation of muscle.

Source page: https://510kreport.com/device/K102375
Methodology: https://510kreport.com/methodology