Physio-Control Corp. is one of 5565 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Physio-Control Corp. - FDA 510(k) Cleared Devices
Recent clearances: LIFEPAK 12 BIPHASIC, NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM, LIFEPAK 500 BIPHASIC
80
Total
78
Cleared
0
Denied
Physio-Control Corp. has 78 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 78 cleared submissions from 1976 to 1999.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Physio-Control Corp.
80 devices
Cleared
Sep 03, 1999
LIFEPAK 12 BIPHASIC
Cardiovascular
88d
Cleared
Sep 01, 1999
NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR...
Cardiovascular
210d
Cleared
May 05, 1999
LIFEPAK 500 BIPHASIC
Cardiovascular
222d
Cleared
Jan 09, 1998
LIFE PAK 12
Cardiovascular
116d
Cleared
Nov 06, 1997
LIFEPAK 300
Cardiovascular
505d
Cleared
Nov 04, 1996
LIFEPAK 500
Cardiovascular
312d
Cleared
Jan 11, 1996
PEDIATRIC QUIK-COMBO
Cardiovascular
189d
Cleared
Dec 29, 1995
LIFEPAK 11
Cardiovascular
267d
Cleared
Sep 26, 1995
LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER, AND LIFEPAK 11 CARDIAC MONITOR
Cardiovascular
321d
Cleared
Feb 03, 1995
QUIK COMBO
Cardiovascular
210d
Cleared
Dec 07, 1994
FAST-PATCH
Cardiovascular
229d
Cleared
Jun 08, 1994
LIFEPAK 300 AUTOMATIC ADVISORY DEFRILLATOR
Cardiovascular
579d
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