# K030382: Selitherm, Model C100

- Pathway: 510(k) (Traditional)
- Applicant: Selicor, Inc.
- Decided: Apr 1, 2003 after 55 days
- Product code: IMJ (Diathermy, Shortwave, For Use In Applying Therapeutic Deep Heat)
- Device class: 2
- Regulation: 21 CFR 890.5290
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
62 later devices descend from it; 1 cites it directly.
0 of 63 devices 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.

## Most influential descendants
- K083433: Intelect SWD 100, Model 1600; Senior Solutions Shortwave Diathermy, Model 1601 (2009), 61 descendants of its own
- K090221: Reaction System (2009), 54 descendants of its own
- K133837: Viora V-Total (2014), 33 descendants of its own
- K142093: V20 System (2014), 32 descendants of its own
- K150035: V10 system (2015), 31 descendants of its own

## Indications for use
Diathermy Component. To generate deep heating within body tissues for the treatment of conditions such as relief of pain, muscle spasms, and joint contractures. Muscle Stimulator Component To increase local blood flow, muscle re-education, relaxation of muscle spasms, prevention or retardation of disuse atrophy, arid immediate post surgical stimulation of calves to prevent deep vein thrombosis.

Source page: https://510kreport.com/device/K030382
Methodology: https://510kreport.com/methodology