# Nfocus Neuromedical, Inc.

- Location (FDA's records): Palo Alto, CA
- FDA decisions: 2 (2009–2010): 2 510(k) clearances
- Product codes: KRD (1), DQY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K091952: Acta Vessel Occlusion System (Vos) (Sep 10, 2010)
- K090918: Nfocus Neuromedical Echo Distal Access Catheter (Jul 30, 2009)

Source page: https://510kreport.com/company/nfocus-neuromedical