# Cardio Design Pty., Ltd.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 2 (1996–1998): 2 510(k) clearances
- Product codes: HIR (2)
- Predicates its devices cite: 0 (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 that cite its devices most
- Advanced Tactile Imaging, Inc.: 1 (https://510kreport.com/company/advanced-tactile-imaging)
- Utah Medical Products, Inc.: 1 (https://510kreport.com/company/utah-medical-products)

## Its most-cited devices
- K945611: Peritron (1996), cited by 1
- K983052: Peritron Perineometer Model 9300V or 9300A (1998), cited by 1

## Recent decisions
- K983052: Peritron Perineometer Model 9300V or 9300A (Oct 19, 1998)
- K945611: Peritron (Feb 8, 1996)

Source page: https://510kreport.com/company/cardio-design