# St. Jude Medical, Inc.-Endocardial Solutions

- Location (FDA's records): St. Paul, MN
- FDA decisions: 1 (2006–2006): 1 510(k) clearance
- Product codes: DQK (1)
- Predicates its devices cite: 1 (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
- Endocardial Solutions, Inc.: 1 (https://510kreport.com/company/endocardial-solutions)

## Firms that cite its devices most
- Biosense Webster, Inc.: 1 (https://510kreport.com/company/biosense-webster)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

## Its most-cited devices
- K060954: Modification to Ensite System, Model EE3000 (2006), cited by 2

## Recent decisions
- K060954: Modification to Ensite System, Model EE3000 (Apr 21, 2006)

Source page: https://510kreport.com/company/st-jude-medical-endocardial-solutions