# K932299: Electro-Mesh

- Pathway: 510(k) (Traditional)
- Applicant: Prizm Medical, Inc.
- Decided: Jul 1, 1994 after 416 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
31 later devices descend from it; 2 cite it directly.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K053214: Theraknit Garment Electrode (2005), 29 descendants of its own
- K103719: Lifecare Conductive Garments (2011), 20 descendants of its own
- K123354: Revitive IX (2013), 19 descendants of its own
- K143207: Revitive IX (OTC) (2015), 17 descendants of its own
- K151834: BEMER Classic Set, BEMER Pro-Set (2017), 11 descendants of its own

Source page: https://510kreport.com/device/K932299
Methodology: https://510kreport.com/methodology