# Medtronic Cardiac Surgery, Medtronic, Inc.

- Location (FDA's records): Anaheim, CA
- FDA decisions: 2 (1996–1996): 2 510(k) clearances
- Product codes: DQX (1), DTL (1)
- Predicates its devices cite: 5 (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
- Gish Biomedical, Inc.: 2 (https://510kreport.com/company/gish-biomedical)
- Electromedics, Inc.: 1 (https://510kreport.com/company/electromedics)
- Scimed: 1 (https://510kreport.com/company/scimed)
- Sorin Biomedica, Fiat, USA, Inc.: 1 (https://510kreport.com/company/sorin-biomedica-fiat-usa)

## Firms that cite its devices most
- Medtronic Bio-Medicus, Inc.: 1 (https://510kreport.com/company/medtronic-bio-medicus)
- Minntech Corp.: 1 (https://510kreport.com/company/minntech)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Medtronic Perfusion Systems: 1 (https://510kreport.com/company/medtronic-perfusion-systems)

## Its most-cited devices
- K960755: Cardiotherm Blood Cardioplegia Systems (1996), cited by 3
- K953564: Medtronic Overpressure/Vacuum Relief Valve (1996), cited by 1

## Recent decisions
- K960755: Cardiotherm Blood Cardioplegia Systems (May 23, 1996)
- K953564: Medtronic Overpressure/Vacuum Relief Valve (Feb 2, 1996)

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