# K944260: Ecg Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Msb, Ltd.
- Decided: Jul 7, 1995 after 311 days
- Product code: DRX (Electrode, Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2360
- 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
- K030509: Skintact Ecg Tab Electrode (2003), 4 descendants of its own
- K040784: Protab Ecg Tabb Electrode (2004), 1 descendant of its own
- K101685: IP-SET (2010), 0 descendants of its own
- K093327: Intco Tab Electrode (2010), 0 descendants of its own
- K090496: Qwiklead Reusable Electrocardiograph Electrode Patch (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K944260
Methodology: https://510kreport.com/methodology