Medtronic Emergency Response Systems, Inc. - FDA 510(k) Cleared Devic...
6
Total
6
Cleared
0
Denied
Medtronic Emergency Response Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 6 cleared submissions from 2004 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Emergency Response Systems, Inc. Filter by specialty or product code using the sidebar.
6 devices
Cleared
Jan 26, 2007
LIFEPAK 12 DEFIBRILLATOR/MONITOR
Cardiovascular
67d
Cleared
Dec 22, 2006
LIFEPAK 20 DEFIBRILLATOR/ MONITOR
Cardiovascular
71d
Cleared
Feb 17, 2006
LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
Cardiovascular
203d
Cleared
Jan 20, 2006
LIFENET EXCHANGE SYSTEM
Cardiovascular
101d
Cleared
Dec 22, 2005
LIFEPAK, MODEL 1000
Cardiovascular
475d
Cleared
Jul 01, 2004
LIFEPAK 12 DEFIBRILLATOR/MONITOR
Cardiovascular
29d