# K150175: HeatLux Pro I

- Pathway: 510(k) (Special)
- Applicant: Home Skinovations, Ltd.
- Decided: Mar 31, 2015 after 64 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: 6 generations back to K974468 (1998). 15 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120582: Heatlux, Home Skinovations, Ltd. (2012) Summary page 5.

## Most influential descendants
- K152087: HeatLux Pro II (2016), 0 descendants of its own

## Indications for use
HeatLux Pro I is over the counter hand held device intended to emit energy in the visible and near IR spectrum to provide topical heating for the purpose of elevating tissue temperature for a temporary relief of minor muscular and joint pain and stiffness, minor arthritis pain or muscle spasm, the temporary increase in local and blood circulation, and temporary relaxation of muscles.

Source page: https://510kreport.com/device/K150175
Methodology: https://510kreport.com/methodology