# Medrad Interventional/Possis

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 2 (2010–2011): 2 510(k) clearances
- Product codes: QEZ (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Possis Medical, Inc.: 2 (https://510kreport.com/company/possis-medical)

## Firms that cite its devices most
- Medrad, Inc.: 2 (https://510kreport.com/company/medrad)

## Its most-cited devices
- K101406: Angiojet Solent Proxi Thrombectomy Set Model 109676-001 (2010), cited by 2

## Recent decisions
- K101354: Fetch 2 Aspiration Catheter Model 109400-001 (Jan 21, 2011)
- K101406: Angiojet Solent Proxi Thrombectomy Set Model 109676-001 (Jun 16, 2010)

Source page: https://510kreport.com/company/medrad-interventional-possis