Medical Device Manufacturer · US , Minneapolis , MN

Medrad Interventional/Possis - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Medrad Interventional/Possis has 2 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Medrad Interventional/Possis Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Medrad Interventional/Possis

2 devices
1-2 of 2
Cleared Jan 21, 2011
FETCH 2 ASPIRATION CATHETER MODEL 109400-001
K101354 · QEZ
Cardiovascular · 252d
Cleared Jun 16, 2010
ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001
K101406 · QEZ
Cardiovascular · 28d
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