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FDA 510(k) Applications Submitted by SHERRI POCOCK
FDA 510(k) Number
Submission Date
Device Name
Applicant
K052057
07/29/2005
LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
K042404
09/03/2004
LIFEPAK, MODEL 1000
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
K010918
03/27/2001
LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM
MEDTRONIC PHYSIO-CONTROL CORP.
K011144
04/16/2001
LIFEPAK 600 AUTOMATED EXTERNAL DEFIBRILLATOR
MEDTRONIC PHYSIO-CONTROL CORP.
K962359
06/19/1996
LIFEPAK 300
PHYSIO-CONTROL CORP.
K012274
07/19/2001
MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER
MEDTRONIC PHYSIO-CONTROL CORP.
K012428
07/31/2001
MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
MEDTRONIC PHYSIO-CONTROL CORP.
K022732
08/16/2002
INFANT/CHILD REDUCED ENERGY ELECTRODES
MEDTRONIC PHYSIO-CONTROL CORP.
K973486
09/15/1997
LIFE PAK 12
PHYSIO-CONTROL CORP.
K983393
09/25/1998
LIFEPAK 500 BIPHASIC
PHYSIO-CONTROL CORP.
K955854
12/28/1995
LIFEPAK 500
PHYSIO-CONTROL CORP.
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