# K032787: Neurolase, Models 150V, 150C, 1064

- Pathway: 510(k) (Traditional)
- Applicant: Spectrum Laser & Technologies
- Decided: Nov 20, 2003 after 73 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 K875052 (1988). 12 ancestors in all.
15 later devices descend from it; 4 cite it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001179: Super Nova, Acubeam, Light Force Therapy, Inc. (2000)
- K020017: Medx 1000 Series, Medx Electronics, Inc. (2002)
- K974468: Photonic Stimulator, Bales Scientific, Inc. (1998) Summary page 1.
- K024179: Palomar Lightcube, Palomar Medical Products, Inc. (2003)
- K982546: Phaser-2000, Diomedics, Inc. (1998) Summary page 1.

## Most influential descendants
- K033986: MLT-1000 IR Laser System (2004), 10 descendants of its own
- K053473: Maestro MDTL Laser System (2006), 8 descendants of its own
- K061656: Laser-D68 (2006), 5 descendants of its own
- K120604: K-Laser (2012), 4 descendants of its own
- K082969: Luminex Infrared Lamp System (2008), 1 descendant of its own

## Indications for use
The Neurolase devices are an infrared lamp per 21 CFR 890.5500 that emit energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature to provide temporary relief of minor muscles and joint pain and stiffness, minor pain and stiffness associated with arthritis, or muscle spasm. These devices may temporarily increase blood circulation, and may be used to promote relaxation of muscle tissue.

Source page: https://510kreport.com/device/K032787
Methodology: https://510kreport.com/methodology