Medical Device Manufacturer · US , Minneapolis , MN

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

2 submissions · 2 cleared · Since 2010

Recent clearances: FETCH 2 ASPIRATION CATHETER MODEL 109400-001, ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

View 2 510(k) Devices ↓

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

Cardiovascular · 252d

Cleared Jun 16, 2010

ANGIOJET SOLENT PROXI THROMBECTOMY SET MODEL 109676-001

Cardiovascular · 28d