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.