# Epicor Medical, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 2 (2004–2004): 2 510(k) clearances
- Product codes: NTB (2)
- Predicates its devices cite: 16 (1 its own); citations of its devices by later devices: 5 (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
- Boston Scientific Corp: 4 (https://510kreport.com/company/boston-scientific)
- Afx, Inc.: 4 (https://510kreport.com/company/afx)
- Cardiofocus, Inc.: 3 (https://510kreport.com/company/cardiofocus)
- AtriCure, Inc.: 2 (https://510kreport.com/company/atricure)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Cardima, Inc.: 1 (https://510kreport.com/company/cardima)

## Firms that cite its devices most
- St Jude Medical: 2 (https://510kreport.com/company/st-jude-medical)
- AtriCure, Inc.: 1 (https://510kreport.com/company/atricure)
- Ultrazonix Dnt AB: 1 (https://510kreport.com/company/ultrazonix-dnt)

## Its most-cited devices
- K040641: Ultracinch Ablation Device, Ultracinch Accessory Pack, Models UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-Acc-1 (2004), cited by 3
- K022894: Epicor Medical Ablation System (2004), cited by 2

## Recent decisions
- K040641: Ultracinch Ablation Device, Ultracinch Accessory Pack, Models UC-8, UC-9, UC-10, UC-11, UC-12, UC-13, UC-14, UC-Acc-1 (May 5, 2004)
- K022894: Epicor Medical Ablation System (Feb 26, 2004)

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