# Cardioinsight Technologies, Inc.

- Location (FDA's records): Cleveland, OH
- FDA decisions: 3 (2014–2016): 3 510(k) clearances
- Product codes: DQK (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 5 (2 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
- C.R. Bard Inc., Bard Electrophysiology Division: 1 (https://510kreport.com/company/cr-bard-bard-electrophysiology-division)

## Firms that cite its devices most
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)
- Corify Care S.L: 1 (https://510kreport.com/company/corify-care-s-l)
- Catheter Precision, Inc.: 1 (https://510kreport.com/company/catheter-precision)

## Its most-cited devices
- K162440: CardioInsight Cardiac Mapping System (2016), cited by 3
- K150990: ECVUE Mapping System (2015), cited by 1
- K140497: Ecvue Mapping System (2014), cited by 1

## Recent decisions
- K162440: CardioInsight Cardiac Mapping System (Nov 4, 2016)
- K150990: ECVUE Mapping System (Jul 2, 2015)
- K140497: Ecvue Mapping System (Nov 19, 2014)

Source page: https://510kreport.com/company/cardioinsight-technologies