10,000 results · 116ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PHYSIO CONTROL INC.

FDA Adverse Event
Other ·PHYSIO-CONTROL INC.·Product code MKJ·October 19, 2016

LUCAS CPR CHEST COMPRESSION SYSTEM

FDA Adverse Event
Malfunction ·JOLIFE AB·Product code DRM·July 1, 2014

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·October 17, 2007

PHYSIO-CONTROL, INC LIFEPAK 12 MONITOR

FDA Adverse Event
Death ·PHYSIO-CONTROL, INC.·Product code LDD·July 21, 2009

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 16, 2007

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·October 16, 2007

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·October 22, 2007

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·December 5, 2007

LIFEPAK (R) 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Death ·PHYSIO-CONTROL, INC.·Product code MKJ·October 16, 2005

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·December 5, 2007

LIFEPAN 9P DEFIBRILLATOR/MONITOR/PACEMAKER

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·December 5, 2007

LIFEPAK CR(R) PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 20, 2007

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·September 5, 2007

LIFEPAK CR PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 20, 2007

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Injury ·PHYSIO-CONTROL, INC.·Product code MKJ·December 4, 2007

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·November 29, 2007

LIFEPAK CR(R) PLUS DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·October 1, 2007

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·December 7, 2007

LIFEPAK 20 DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·December 4, 2007

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 20, 2007