# Diacardio, Ltd.

- Location (FDA's records): Somerset, MA
- FDA decisions: 2 (2013–2016): 2 510(k) clearances
- Product codes: LLZ (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 4 (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
- Siemens Medical Solutions USA, Inc., Ultrasound DI: 2 (https://510kreport.com/company/siemens-medical-solutions-usa-ultrasound-di)
- Philips Ultrasound, Inc.: 1 (https://510kreport.com/company/philips-ultrasound)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Firms that cite its devices most
- Ultralinq Healthcare Solutions, Inc.: 1 (https://510kreport.com/company/ultralinq-healthcare-solutions)
- GE Medical Systems Ultrasound and Primary Care Diagnostics: 1 (https://510kreport.com/company/ge-medical-systems-ultrasound-and-primary-care-diagnostics)
- Bay Labs, Inc.: 1 (https://510kreport.com/company/bay-labs)

## Its most-cited devices
- K130779: Lvivo EF System (2013), cited by 4

## Recent decisions
- K161382: LVivo Software Application (Jul 28, 2016)
- K130779: Lvivo EF System (Aug 15, 2013)

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