Medical Device Manufacturer · US , Redmond , WA

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

8 submissions · 6 cleared · Since 2001

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

1-8 of 8

Cleared Apr 23, 2004

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