# K945836: 1800 Monitoring Ecg Electrode and 1870 Diaphoretic Monitoring Ecg Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Conmed Andover Medical, Inc.
- Decided: Jun 20, 1995 after 203 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K091856: Conmed Ecg Monitoring Electrodes , Model 1700 ( Including 2500), 1750, 2700, 2710, 1800, Series (2009), 0 descendants of its own

Source page: https://510kreport.com/device/K945836
Methodology: https://510kreport.com/methodology