Medical Device Manufacturer · US , Sunnyvale , CA

Medtronic Percusurge, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2002
2
Total
2
Cleared
0
Denied

Medtronic Percusurge, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 2 cleared submissions from 2002 to 2002. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Medtronic Percusurge, Inc.
2 devices
1-2 of 2
Cleared Nov 15, 2002
PERCUSURGE GUARDWIRE PLUS TEMPORARY OCCLUSION AND ASPIRATION SYSTEM
K013913 · NFA
Cardiovascular · 353d
Cleared Jan 25, 2002
MODIFICATION TO GUARDWIRE PLUS TEMPORARY OCCLUSION & ASPIRATION SYSTEM
K014223 · NFA
Cardiovascular · 30d
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