# Medtronic Cardiorhythm

- Location (FDA's records): San Jose, CA
- FDA decisions: 5 (1994–1998): 5 510(k) clearances
- Product codes: DRF (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 21 (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 that cite its devices most
- Alliance Medical Corp.: 8 (https://510kreport.com/company/alliance-medical)
- Medtronic, Inc.: 4 (https://510kreport.com/company/medtronic)
- Medtronic Vascular: 3 (https://510kreport.com/company/medtronic-vascular)
- Sterilmed, Inc.: 2 (https://510kreport.com/company/sterilmed)
- Innovative Health, LLC: 2 (https://510kreport.com/company/innovative-health)
- Biotronik, Inc.: 1 (https://510kreport.com/company/biotronik)
- Cardima, Inc.: 1 (https://510kreport.com/company/cardima)

## Its most-cited devices
- K931794: Marinr Series EP Diagnostic Catheters (1994), cited by 7
- K981642: Stablemapr Steerable Intracardiac Catheters (1998), cited by 6
- K951347: Marinr Series EP Diagnosti Catheters (1995), cited by 4
- K964272: Performr Series EP Diagnostic Catheters (1997), cited by 2
- K953185: Platinum Series EP Diagnostic Catheters (1996), cited by 2

## Recent decisions
- K981642: Stablemapr Steerable Intracardiac Catheters (Aug 5, 1998)
- K964272: Performr Series EP Diagnostic Catheters (Jan 23, 1997)
- K953185: Platinum Series EP Diagnostic Catheters (Apr 15, 1996)
- K951347: Marinr Series EP Diagnosti Catheters (May 10, 1995)
- K931794: Marinr Series EP Diagnostic Catheters (Jun 6, 1994)

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