# K070338: Rainbow, Rainbow Light,Rainbow Blue, Rainbow Plus

- Pathway: 510(k) (Traditional)
- Applicant: Rainbow Communications, Inc.
- Decided: Aug 28, 2007 after 204 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
RainbowTM, Rainbow LightTM, Rainbow BlueTM, Rainbow PlusTM Portable LED Phototherapy Devices are for an ordinary person's home-use without additional assistance from professionals to emit light energy to the body and skin for the purpose of for the temporary relief of minor muscle and joint pain, arthritis and muscle spasm, relieving stiffness, promoting relaxation of muscle tissue, and temporarily increasing local blood circulation where light is applied.

Source page: https://510kreport.com/device/K070338
Methodology: https://510kreport.com/methodology