Medtronic Physio-Control Corp. is one of 18143 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Physio-Control Corp. - FDA 510(k) Cleared Devices
Recent clearances: LIFEPAK 12, LIFEPAK 12, 20, 500, CR PLUS, INFANT/CHILD REDUCED ENERGY ELECTRODES
8
Total
6
Cleared
0
Denied
Medtronic Physio-Control Corp. has 6 FDA 510(k) cleared medical devices. Based in Redmond, US.
Historical record: 6 cleared submissions from 2001 to 2004. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Physio-Control Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic Physio-Control Corp.
8 devices
Cleared
Apr 23, 2004
LIFEPAK 12
Cardiovascular
28d
Cleared
Nov 06, 2003
LIFEPAK 12, 20, 500, CR PLUS
Cardiovascular
27d
Cleared
Dec 13, 2002
INFANT/CHILD REDUCED ENERGY ELECTRODES
Cardiovascular
119d
Cleared
Feb 05, 2002
MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKER
Cardiovascular
201d
Cleared
Dec 03, 2001
LIFEPAK 600 AUTOMATED EXTERNAL DEFIBRILLATOR
Cardiovascular
231d
Cleared
Sep 28, 2001
MODIFICATION TO: LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
Cardiovascular
59d
Cleared
Aug 23, 2001
LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM
Cardiovascular
149d
Cleared
Jan 31, 2001
LIFEPAK 12DEFIBERLLATOR/MONITOR SERIES
Cardiovascular
175d