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

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

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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