# Cerus Endovascular, Inc.

- Location (FDA's records): Fremont, CA
- FDA decisions: 2 (2019–2022): 2 510(k) clearances
- Product codes: DQY (1), QJP (1)
- Predicates its devices cite: 2 (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

## Firms whose devices it cites most
- MicroVention, Inc.: 2 (https://510kreport.com/company/microvention)

## Recent decisions
- K213314: CerusEndo Microcatheter (027) (Mar 15, 2022)
- K182487: CerusEndo Microcatheter (Jul 20, 2019)

Source page: https://510kreport.com/company/cerus-endovascular