# K043047: Dynatron Ibox Iontophoresis Device

- Pathway: 510(k) (Traditional)
- Applicant: Dynatronics Corp.
- Decided: Jan 7, 2005 after 64 days
- Product code: EGJ (Device, Iontophoresis, Other Uses)
- Device class: 2
- Regulation: 21 CFR 890.5525
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K912015 (1991). 10 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K863166: Model 6110 Iontophoretic Applicator, Life-Tech Intl., Inc. (1987) Summary page 1.
- K913601: Microphor, Life-Tech Intl., Inc. (1994) Summary page 3.
- K031115: RH-900, Iomed, Inc. (2003) Summary page 3.
- K915444: Dupel Iontophoresis Device, Empi (1994) Summary page 1.

## Most influential descendants
- K170291: IontoDC (2017), 0 descendants of its own

## Indications for use
The Dynatron® IBoxTM is intended to use a direct current to introduce ions of soluble salts or other drugs into the body.

Source page: https://510kreport.com/device/K043047
Methodology: https://510kreport.com/methodology