# Quinton Cardiology, Inc.

- Location (FDA's records): Bothell, WA
- FDA decisions: 1 (2004–2004): 1 510(k) clearance
- Product codes: MHX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Quinton, Inc.: 1 (https://510kreport.com/company/quinton)

## Firms that cite its devices most
- Medicalgorithmics S.A.: 1 (https://510kreport.com/company/medicalgorithmics)
- Scottcare Corporation: 1 (https://510kreport.com/company/scottcare)

## Its most-cited devices
- K041607: Quinton Q-TE; RMS (2004), cited by 2

## Recent decisions
- K041607: Quinton Q-TE; RMS (Jul 16, 2004)

Source page: https://510kreport.com/company/quinton-cardiology