# Graftcath, Inc.

- Location (FDA's records): Eden Prarie, MN
- FDA decisions: 1 (2008–2008): 1 510(k) clearance
- Product codes: DSY (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (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
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Edwards Lifesciences, LLC: 1 (https://510kreport.com/company/edwards-lifesciences)

## Firms that cite its devices most
- Hemosphere, Inc.: 3 (https://510kreport.com/company/hemosphere)
- Hemoshpere, Inc., A Cryolife Company: 1 (https://510kreport.com/company/hemoshpere-a-cryolife)

## Its most-cited devices
- K071778: Hero Vascular Access Device (2008), cited by 4

## Recent decisions
- K071778: Hero Vascular Access Device (Jan 30, 2008)

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