Medical Device Manufacturer · US , Redmond , WA

Medtronic Emergency Response Systems, Inc. - FDA 510(k) Cleared Devic...

6 submissions · 6 cleared · Since 2004

Recent clearances: LIFEPAK 12 DEFIBRILLATOR/MONITOR, LIFEPAK 20 DEFIBRILLATOR/ MONITOR, LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medtronic Emergency Response Systems, Inc. Cardiovascular ✕

6 devices

1-6 of 6

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