# Medtronic Emergency Response Systems, Inc.

- Location (FDA's records): Redmond, WA
- FDA decisions: 6 (2004–2007): 6 510(k) clearances
- Product codes: MKJ (5), MSX (1)
- Predicates its devices cite: 26 (1 its own); citations of its devices by later devices: 11 (1 its own)
- Recalls linked to its devices: 12 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medtronic Physio-Control Corp.: 13 (https://510kreport.com/company/medtronic-physio-control)
- Physio-Control Corp.: 9 (https://510kreport.com/company/physio-control)
- Philips Medical Systems, Inc.: 3 (https://510kreport.com/company/philips-medical-systems)

## Firms that cite its devices most
- Physio-Control Corp.: 7 (https://510kreport.com/company/physio-control)
- Heartsine Technologies, Inc.: 1 (https://510kreport.com/company/heartsine-technologies)
- Amco International Manufacturing & Design, Inc.: 1 (https://510kreport.com/company/amco-international-manufacturing-design)
- Ad Elektronik GmbH: 1 (https://510kreport.com/company/ad-elektronik)

## Its most-cited devices
- K041459: Lifepak 12 Defibrillator/Monitor (2004), cited by 4
- K063119: Lifepak 20 Defibrillator/ Monitor (2006), cited by 2
- K052057: Lifepak 500 Automated External Defibrillator (2006), cited by 2
- K063510: Lifepak 12 Defibrillator/Monitor (2007), cited by 2
- K042404: Lifepak, Model 1000 (2005), cited by 1

## Recent decisions
- K063510: Lifepak 12 Defibrillator/Monitor (Jan 26, 2007)
- K063119: Lifepak 20 Defibrillator/ Monitor (Dec 22, 2006)
- K052057: Lifepak 500 Automated External Defibrillator (Feb 17, 2006)
- K052854: Lifenet Exchange System (Jan 20, 2006)
- K042404: Lifepak, Model 1000 (Dec 22, 2005)
- K041459: Lifepak 12 Defibrillator/Monitor (Jul 1, 2004)

Source page: https://510kreport.com/company/medtronic-emergency-response-systems