# K061849: Mesoderm

- Pathway: 510(k) (Traditional)
- Applicant: Aa Advanced Technology, Inc.
- Decided: Apr 30, 2007 after 304 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: 3 generations back to K863166 (1987). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032968: Trsansderm Ionto System, Mattioli Engineering Corp. (2003) Summary page 1.
- K042590: Transderm Ionto System, MK 2, Mattioli Engineering Corp. (2004) Summary page 1.

## Most influential descendants
- K083016: Acthyderm (2009), 0 descendants of its own

## Indications for use
MesoDerm is indicated for the administration of soluble salts or other drugs into the body for medical purposes as an alternative to hypodermic injections.

Source page: https://510kreport.com/device/K061849
Methodology: https://510kreport.com/methodology