# K020227: Selicor, Models A100 & D100

- Pathway: 510(k) (Traditional)
- Applicant: Selicor, Inc.
- Decided: Jul 30, 2002 after 189 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.
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
Diathermy Component, To generate deep heating within-body tissues for the treatment of conditions such as relief of pain, muscle spasms, and joint contractures.

Source page: https://510kreport.com/device/K020227
Methodology: https://510kreport.com/methodology