# Qardio, Inc.

- Location (FDA's records): San Fransciso, CA
- FDA decisions: 3 (2014–2022): 3 510(k) clearances
- Product codes: DXN (2), DSH (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- iRhythm Technologies, Inc.: 1 (https://510kreport.com/company/irhythm-technologies)
- Andon Health Co, Ltd.: 1 (https://510kreport.com/company/andon-health)
- Ya Horng Electronic Co., Ltd.: 1 (https://510kreport.com/company/ya-horng-electronic)

## Firms that cite its devices most
- Fudakang Industrial Co., Ltd.: 1 (https://510kreport.com/company/fudakang-industrial)
- Fourth Frontier Technologies Pvt, Ltd.: 1 (https://510kreport.com/company/fourth-frontier-technologies-pvt)

## Its most-cited devices
- K140067: Qardioarm (2014), cited by 2
- K201644: QardioCore (2021), cited by 1

## Recent decisions
- K220106: QardioArm 2 (Jun 15, 2022)
- K201644: QardioCore (Feb 28, 2021)
- K140067: Qardioarm (Jun 18, 2014)

Source page: https://510kreport.com/company/qardio