# Conmed Andover Medical, Inc.

- Location (FDA's records): Haverhill, MA
- FDA decisions: 8 (1994–1995): 8 510(k) clearances
- Product codes: DRX (6), DSA (1), GXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Conmed Corporation: 4 (https://510kreport.com/company/conmed)

## Its most-cited devices
- K944849: 2700 Cleartrace Radiotranslucent Monitoring Ecg Electrobe (1994), cited by 1
- K944655: Ecg Electrode (1994), cited by 1
- K945836: 1800 Monitoring Ecg Electrode and 1870 Diaphoretic Monitoring Ecg Electrodes (1995), cited by 1
- K946273: 1700 Monitoring Ecg Electrode (1995), cited by 1

## Recent decisions
- K945836: 1800 Monitoring Ecg Electrode and 1870 Diaphoretic Monitoring Ecg Electrodes (Jun 20, 1995)
- K946273: 1700 Monitoring Ecg Electrode (May 17, 1995)
- K944655: Ecg Electrode (Nov 22, 1994)
- K944726: 1710 Monitoring Ecg Electrode (Nov 22, 1994)
- K944849: 2700 Cleartrace Radiotranslucent Monitoring Ecg Electrobe (Oct 17, 1994)
- K942718: Cloth Tens/Bnes Electrode (Sep 22, 1994)
- K941839: Disposable Surgical Cable (Jul 27, 1994)
- K942925: Conmed Andover Med Ecg Electrodes (Jul 20, 1994)

Source page: https://510kreport.com/company/conmed-andover-medical