# K091856: Conmed Ecg Monitoring Electrodes , Model 1700 ( Including 2500), 1750, 2700, 2710, 1800, Series

- Pathway: 510(k) (Special)
- Applicant: Conmed Corporation
- Decided: Aug 7, 2009 after 45 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
Longest line of descent: 1 generation back to K944849 (1994). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954388: Conmed 2710 Cleartrace 2 LT Monitoring Ecg Electrode, Conmedcorp (1996) Summary page 2.
- K944849: 2700 Cleartrace Radiotranslucent Monitoring Ecg Electrobe, Conmed Andover Medical, Inc. (1994) Summary page 2.
- K944655: Ecg Electrode, Conmed Andover Medical, Inc. (1994) Summary page 2.
- K945836: 1800 Monitoring Ecg Electrode and 1870 Diaphoretic Monitoring Ecg Electrodes, Conmed Andover Medical, Inc. (1995) Summary page 2.
- K946273: 1700 Monitoring Ecg Electrode, Conmed Andover Medical, Inc. (1995) Summary page 2.

## Indications for use
The ConMed ECG Monitoring Electrodes are pre-gelled, single patient use, disposable electrocardiographic electrodes for use as an accessory to ECG equipment for long term or short term monitoring and diagnostic procedures with regular or diaphoretic adhesives.

Source page: https://510kreport.com/device/K091856
Methodology: https://510kreport.com/methodology