# K022950: Miniphysionizer 2.0 and Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Physion, Inc.
- Decided: Apr 18, 2003 after 225 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
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
The Miniphysionzier 2.0 and Electrodes are intended for use in the iontophoretic transdermal administration of ionized medications.

Source page: https://510kreport.com/device/K022950
Methodology: https://510kreport.com/methodology