Medical Device Manufacturer · US , Minneapolis , MN

Medtronic Inc. Cardiac Rhythm Management - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004
2
Total
2
Cleared
0
Denied

Medtronic Inc. Cardiac Rhythm Management has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 2004 to 2007. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medtronic Inc. Cardiac Rhythm Management Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medtronic Inc. Cardiac Rhythm Management
2 devices
1-2 of 2
Cleared Mar 15, 2007
ATTAIN HYBRID GUIDE WIRES, MODEL GWR419378, GWR419388, GWR419478, GWR419488
K063210 · DQX
Cardiovascular · 143d
Cleared Jan 22, 2004
MEDTRONIC SELECTSITE DEFLECTABLE CATHETER SYSTEM, MODELS C304-S59 AND C304-L69
K033989 · DQY
Cardiovascular · 30d
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