# K082969: Luminex Infrared Lamp System

- Pathway: 510(k) (Traditional)
- Applicant: Medical Laser Systems, Inc.
- Decided: Oct 23, 2008 after 17 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 K875052 (1988). 18 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033923: TH0R Ddii IR Lamp System, Thor Intl. (2004) Summary page 2.
- K053473: Maestro MDTL Laser System, Advanced Medical Technologies, Inc. (2006) Summary page 2.
- K040662: Vectra Genisys (Module & Transportable) and Intelect XT (Module & Transportable) Laser Systems, Chattanooga Group (2004) Summary page 2.

## Most influential descendants
- K123177: Stimlase 2000 Low Level Laser Therapy System (2013), 0 descendants of its own

## Indications for use
The Luminex Infrared Lamp System is intended to emit energy in the visible and near 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/K082969
Methodology: https://510kreport.com/methodology