# K941799: Disposable Cutaneous Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Bio-Logic Systems Corp.
- Decided: Feb 3, 1995 after 297 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.
6 later devices descend from it; 2 cite it directly.
0 of 7 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
- K052188: Cutaneous Electrode (2005), 5 descendants of its own
- K110289: Friendship Medical Disposable Pre-Gelled AG / Agcl Surface Electrode (2011), 2 descendants of its own
- K142159: Disposable Pre-Gelled Surface Electrode (2015), 1 descendant of its own
- K203079: MR Conditional Sticky Pad Electrode (2021), 0 descendants of its own
- K172703: Disposable Snap Electrode (2017), 0 descendants of its own

Source page: https://510kreport.com/device/K941799
Methodology: https://510kreport.com/methodology