# K932454: 3M Red Dot 2330 Resting Ekg Electrode

- Pathway: 510(k) (Traditional)
- Applicant: 3M Health Care, Ltd.
- Decided: Aug 16, 1993 after 87 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K101576: Centerridge Diagnostic Ecg Electrode, Centerridge Monitoring Ecg Electrodes (2010), 0 descendants of its own
- K974445: 3M Red Dot Resting Ekg Electrode, Catalog 2360 (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K932454
Methodology: https://510kreport.com/methodology