# K014208: Ssir System

- Pathway: 510(k) (Traditional)
- Applicant: Russian-American Technology Associates, Inc.
- Decided: Jul 2, 2002 after 193 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Photonic Stimulator: named in the summary without a submission number
- (no number) Super Nova / Acukam systems: named in the summary without a submission number
- (no number) Light Patch: named in the summary without a submission number
- (no number) Nu Photonics Pain Therapist system: named in the summary without a submission number

## Most influential descendants
- K030275: MB System, Bioenergy Light Therapy (2004), 0 descendants of its own

## Indications for use
The SSIR 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 circulation; and / or the temporary relaxation of muscle.

Source page: https://510kreport.com/device/K014208
Methodology: https://510kreport.com/methodology