# Et Medical Devices Spa

- Location (FDA's records): Cavareno, IT
- FDA decisions: 3 (2005–2009): 3 510(k) clearances
- Product codes: DPS (2), MWJ (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 8 (1 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
- H&C Medical Devices Spa: 1 (https://510kreport.com/company/h-c-medical-devices)

## Firms that cite its devices most
- Cardioline S.P.A: 2 (https://510kreport.com/company/cardioline)
- Contec Medical System Co., Ltd.: 2 (https://510kreport.com/company/contec-medical-system)
- Cardiac Science Corporation: 1 (https://510kreport.com/company/cardiac-science)
- Mobhealth Incorporation: 1 (https://510kreport.com/company/mobhealth-incorporation)
- Viasys Healthcare GmbH: 1 (https://510kreport.com/company/viasys-healthcare)

## Its most-cited devices
- K051534: Cardioline AR 600, AR 1200, AR 2100 (2005), cited by 5
- K082124: Carditte Microtel (2009), cited by 3

## Recent decisions
- K091054: WALK400H (Jul 27, 2009)
- K082124: Carditte Microtel (Feb 19, 2009)
- K051534: Cardioline AR 600, AR 1200, AR 2100 (Oct 5, 2005)

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