# K132016: Lumix 3 Plus and Lumix 3 Ultra System

- Pathway: 510(k) (Traditional)
- Applicant: Texas Applied Biomedical Services, Inc.
- Decided: Jun 2, 2014 after 336 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: 3 generations back to K001179 (2000). 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)
- K042256: IR Heat Lamp Systems: Icl 15 HFPL System, Icl 60 Plus HFPL System (Models 40, 100 and 250), Icl 100 Activo Scanner Syste, Usa Laser Biotech, Inc. (2004) Summary page 3.

## Most influential descendants
- K171087: AXON IR Heat Lamp (2017), 0 descendants of its own
- K161198: Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3 (2016), 0 descendants of its own
- K160947: LUMIX CPS 1 IR Lamp System LUMIX CPS 2 IR Lamp System LUMIX CPS 3 IR Lamp System LUMIX CPS 4 IR Lamp System LUMIX CPS 5 IR Lamp System (2016), 0 descendants of its own

## Indications for use
The Lumix 3 100W Plus and Lumix 3 250W Ultra Systems are intended to emit energy in the 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/K132016
Methodology: https://510kreport.com/methodology