# H&C Medical Devices Spa

- Location (FDA's records): Milan, IT
- FDA decisions: 3 (2000–2002): 3 510(k) clearances
- Product codes: DPS (2), DXH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (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
- Card Guard, Ltd.: 1 (https://510kreport.com/company/card-guard)

## Firms that cite its devices most
- Viasys Healthcare GmbH: 1 (https://510kreport.com/company/viasys-healthcare)
- Dailycare Biomedical, Inc.: 1 (https://510kreport.com/company/dailycare-biomedical)
- Et Medical Devices Spa: 1 (https://510kreport.com/company/et-medical-devices)
- Reynolds Medical, Ltd.: 1 (https://510kreport.com/company/reynolds-medical)
- Dyansys, Inc.: 1 (https://510kreport.com/company/dyansys)

## Its most-cited devices
- K002074: AB Cardiette Daedalus View Base and AB Cardiettte Daedalus View Hes (2000), cited by 4
- K012012: Ecg Home (2002), cited by 1

## Recent decisions
- K012012: Ecg Home (Jan 17, 2002)
- K010822: AB Cardiette Start 200 HV (Apr 18, 2001)
- K002074: AB Cardiette Daedalus View Base and AB Cardiettte Daedalus View Hes (Oct 4, 2000)

Source page: https://510kreport.com/company/h-c-medical-devices