# Mivi Neurovascular

- Location (FDA's records): Eden Prarie, MN
- FDA decisions: 2 (2020–2022): 2 510(k) clearances
- Names in FDA's records: Mivi Neurovascular (1); Mivi Neurovascular, Inc. (1)
- Product codes: DQY (1), DXE (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Mivi Neuroscience, Inc.: 1 (https://510kreport.com/company/mivi-neuroscience)
- Penumbra, Inc.: 1 (https://510kreport.com/company/penumbra)

## Firms that cite its devices most
- Mivi Neuroscience, Inc.: 2 (https://510kreport.com/company/mivi-neuroscience)

## Its most-cited devices
- K192558: Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter (2020), cited by 2

## Recent decisions
- K213771: Merlin Aspiration System (Jan 27, 2022)
- K192558: Q3 Distal Access Catheter, Q4 Distal Access Catheter, Q5 Distal Access Catheter, Q6Distal Access Catheter (Apr 6, 2020)

Source page: https://510kreport.com/company/mivi-neurovascular