# Cardiosonix, Ltd.

- Location (FDA's records): Kfar Saba, IL
- FDA decisions: 3 (2002–2004): 3 510(k) clearances
- Product codes: DPW (3)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Biosonix, Ltd.: 2 (https://510kreport.com/company/biosonix)

## Firms that cite its devices most
- Neoprobe Corp.: 2 (https://510kreport.com/company/neoprobe)

## Its most-cited devices
- K030357: Quantix/or Device (2003), cited by 2
- K041180: Quantix or Vessel Stabilizer Device (2004), cited by 1

## Recent decisions
- K041180: Quantix or Vessel Stabilizer Device (Jun 7, 2004)
- K030357: Quantix/or Device (Aug 20, 2003)
- K023431: Quantix/ND Device (Nov 13, 2002)

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