# K060134: Apollo IR Heat Lamp System

- Pathway: 510(k) (Traditional)
- Applicant: Apollo Physical Therapy Products International
- Decided: Mar 21, 2006 after 62 days
- Product code: ILY (Lamp, Infrared, Therapeutic Heating)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K001179 (2000). 33 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 35 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K023621: Bioflex Professional Therapy System, Meditech International, Inc. (2003) Summary page 1.
- K033923: TH0R Ddii IR Lamp System, Thor Intl. (2004) Summary page 1.
- K040729: Solaris D890 Therapy Probe, Dynatronics Corp. (2004) Summary page 1.
- K001179: Super Nova, Acubeam, Light Force Therapy, Inc. (2000) Summary page 1.
- K052647: Clini-Lase System, Models CL-Base, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-Base, CLP-275, CLP-55., American Spine Center, Ltd. (2005) Summary page 1.
- K032787: Neurolase, Models 150V, 150C, 1064, Spectrum Laser & Technologies (2003) Summary page 1.

## Most influential descendants
- K150466: ZX2 Laser System (2015), 0 descendants of its own

## Recalls of this device
- Dec 17, 2014 · Class II · Z-1250-2015: Control units were equipped with an internal mounting kit that does not meet medical safety standards, and are conductive, increasing the risk of electric shock to the user and patient. These units we

## Indications for use
The APOLLO IR Heat Lamp System is 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 promoting relaxation of muscle.

Source page: https://510kreport.com/device/K060134
Methodology: https://510kreport.com/methodology