# Cardiovention, Inc.

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 4 (2002–2003): 4 510(k) clearances
- Product codes: DTQ (2), DTR (1), KFM (1)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 3 (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
- Medtronic Bio-Medicus, Inc.: 1 (https://510kreport.com/company/medtronic-bio-medicus)
- Stockert Instrumente GmbH: 1 (https://510kreport.com/company/stockert-instrumente)
- Jostra Medizintechnik AG: 1 (https://510kreport.com/company/jostra-medizintechnik)

## Firms that cite its devices most
- Medtronic Perfusion Systems: 1 (https://510kreport.com/company/medtronic-perfusion-systems)

## Its most-cited devices
- K012325: Cardiovention Corx System, Model FG 0001 (2002), cited by 2
- K021694: Cardiovention Powerbase Console, Model PBC-100 (2003), cited by 1

## Recent decisions
- K032068: Cardiovention Corx Ios-200 System, Model Ios-200 (Aug 22, 2003)
- K030141: Modification to Cardiovention Powerbase Console, Model PCB-100 (Feb 26, 2003)
- K021694: Cardiovention Powerbase Console, Model PBC-100 (Jan 8, 2003)
- K012325: Cardiovention Corx System, Model FG 0001 (Apr 9, 2002)

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