# St. Jude Medical, Daig Division, Inc.

- Location (FDA's records): Minnetonka, MN
- FDA decisions: 2 (2005–2005): 2 510(k) clearances
- Product codes: DYB (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Daig Corp.: 2 (https://510kreport.com/company/daig)

## Firms that cite its devices most
- St Jude Medical: 2 (https://510kreport.com/company/st-jude-medical)
- Biocardia, Inc.: 1 (https://510kreport.com/company/biocardia)
- Cardiosolutions, Inc.: 1 (https://510kreport.com/company/cardiosolutions)

## Its most-cited devices
- K042623: Agilis Steerable Catheter Introducer, Model 408304 (2005), cited by 4

## Recent decisions
- K051096: Apeel CS Plus Catheter Delivery System, Models 407579, 407580, 407581, 407582 (May 17, 2005)
- K042623: Agilis Steerable Catheter Introducer, Model 408304 (Jan 27, 2005)

Source page: https://510kreport.com/company/st-jude-medical-daig-division