# Neuro Vasx, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 2 (1999–2001): 2 510(k) clearances
- Product codes: DQO (1), KRA (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 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
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Interventional Innovations Corp.: 1 (https://510kreport.com/company/interventional-innovations)
- Target Therapeutics: 1 (https://510kreport.com/company/target-therapeutics)
- Cordis Neurovascular, Inc.: 1 (https://510kreport.com/company/cordis-neurovascular)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)

## Its most-cited devices
- K984258: Neurovasx Sub-Microinfusion Catheter (1999), cited by 1

## Recent decisions
- K011646: Neuroedge Infusion  Catheter (Aug 27, 2001)
- K984258: Neurovasx Sub-Microinfusion Catheter (Feb 11, 1999)

Source page: https://510kreport.com/company/neuro-vasx