# Boston Scientific Epi

- Location (FDA's records): Santa Clara, CA
- FDA decisions: 2 (2003–2004): 2 510(k) clearances
- Product codes: NFA (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 11 (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
- Percu Surge, Inc.: 1 (https://510kreport.com/company/percu-surge)
- Medtronic Percusurge, Inc.: 1 (https://510kreport.com/company/medtronic-percusurge)

## Firms that cite its devices most
- Boston Scientific Corp: 4 (https://510kreport.com/company/boston-scientific)
- Ev3, Inc.: 2 (https://510kreport.com/company/ev3)
- Lumen Biomedical, Inc.: 1 (https://510kreport.com/company/lumen-biomedical)
- Velocimed, Inc.: 1 (https://510kreport.com/company/velocimed)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Its most-cited devices
- K032884: Filter Wire EZ Embolic Protection System and EZ Bent Tip Retrieval Sheath (2004), cited by 7
- K023691: Boston Scientific Filterwire EX Embolic (2003), cited by 4

## Recent decisions
- K032884: Filter Wire EZ Embolic Protection System and EZ Bent Tip Retrieval Sheath (Aug 6, 2004)
- K023691: Boston Scientific Filterwire EX Embolic (Jun 4, 2003)

Source page: https://510kreport.com/company/boston-scientific-epi