# Medtronic Inc. Cardiac Rhythm Management

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 2 (2004–2007): 2 510(k) clearances
- Product codes: DQY (1), DQX (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)
- Cook Vascular, Inc.: 1 (https://510kreport.com/company/cook-vascular)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)
- Arterial Vascular Engineering, Inc.: 1 (https://510kreport.com/company/arterial-vascular-engineering)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Firms that cite its devices most
- Aga Medical Corp.: 2 (https://510kreport.com/company/aga-medical)
- Medtronic, Inc.: 2 (https://510kreport.com/company/medtronic)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Abbott (St. Jude Medical): 1 (https://510kreport.com/company/abbott-st-jude-medical)

## Its most-cited devices
- K033989: Medtronic Selectsite Deflectable Catheter System, Models C304-S59 and C304-L69 (2004), cited by 5
- K063210: Attain Hybrid Guide Wires, Model GWR419378, GWR419388, GWR419478, GWR419488 (2007), cited by 1

## Recent decisions
- K063210: Attain Hybrid Guide Wires, Model GWR419378, GWR419388, GWR419478, GWR419488 (Mar 15, 2007)
- K033989: Medtronic Selectsite Deflectable Catheter System, Models C304-S59 and C304-L69 (Jan 22, 2004)

Source page: https://510kreport.com/company/medtronic-cardiac-rhythm-management