# K003924: Mavidon Medical Electrode Jelly

- Pathway: 510(k) (Traditional)
- Applicant: Mavidon Medical Products
- Decided: Aug 24, 2001 after 247 days
- Product code: GYB (Media, Electroconductive)
- Device class: 2
- Regulation: 21 CFR 882.1275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K111717: Electro-Gel (2012), 8 descendants of its own
- K190050: Tech Dots - Adhesive and conductive gel (2019), 6 descendants of its own
- K192606: SAC2 - Electrode Cream (2020), 2 descendants of its own
- K161715: EndyGel (2017), 2 descendants of its own
- K200402: DR-HO'S Electro Therapy Conductive Gel (2020), 1 descendant of its own

Source page: https://510kreport.com/device/K003924
Methodology: https://510kreport.com/methodology
