# K993123: QK-Wide Band Spectrum Therapeutic Apparatus, Models CO1A, CO1B, CO1C, CO1D, CO2A, CO2B

- Pathway: 510(k) (Traditional)
- Applicant: United Pacific Co., Ltd.
- Decided: Dec 17, 1999 after 88 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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Intented to use to emit energy in the infrafed spectrum to provide topical heating for the purpose of temporarily elevating local tissue temperature. Intended to use for the temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain gpasm, temporary increase in local circulation where applied, and the relaxation of muscle.

Source page: https://510kreport.com/device/K993123
Methodology: https://510kreport.com/methodology