# Cardiarc, Ltd.

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: KPS (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 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
- Segami Corporation: 2 (https://510kreport.com/company/segami)
- Digirad Corp.: 1 (https://510kreport.com/company/digirad)

## Firms that cite its devices most
- Transphoton Corporation: 1 (https://510kreport.com/company/transphoton)
- Spectrum Dynamics, Ltd.: 1 (https://510kreport.com/company/spectrum-dynamics)

## Its most-cited devices
- K053062: Cardiarc Spect Imaging Device, Model CQ103-RV2 (2006), cited by 2

## Recent decisions
- K053062: Cardiarc Spect Imaging Device, Model CQ103-RV2 (Jan 6, 2006)

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