Medical Device Manufacturer · US , Mchenry , IL

Physio-Control Corp. - FDA 510(k) Cleared Devices

80 submissions · 78 cleared · Since 1976

Total

Cleared

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

1-12 of 80

NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR...

K990338 · DXN

Cardiovascular · 210d

Cleared May 05, 1999

LIFEPAK 500 BIPHASIC

K983393 · MKJ

Cardiovascular · 222d

Cleared Jan 09, 1998

LIFE PAK 12

K973486 · MKJ

Cardiovascular · 116d

Cleared Nov 06, 1997

LIFEPAK 300

K962359 · MKJ

Cardiovascular · 505d

Cleared Nov 04, 1996

LIFEPAK 500

K955854 · MKJ

Cardiovascular · 312d

Cleared Jan 11, 1996

PEDIATRIC QUIK-COMBO

K953204 · MKJ

Cardiovascular · 189d

Cleared Dec 29, 1995

LIFEPAK 11

K951593 · DRO

Cardiovascular · 267d

Cleared Sep 26, 1995

LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER, AND LIFEPAK 11 CARDIAC MONITOR

K945511 · MPE

Cardiovascular · 321d

Cleared Feb 03, 1995

QUIK COMBO

K943301 · DRX

Cardiovascular · 210d

Cleared Dec 07, 1994

FAST-PATCH

K941970 · MKJ

Cardiovascular · 229d

Cleared Jun 08, 1994

LIFEPAK 300 AUTOMATIC ADVISORY DEFRILLATOR

K925936 · MKJ

Cardiovascular · 579d

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Physio-Control Corp. - FDA 510(k) Cleared Devices

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