# Cardeon Corp.

- Location (FDA's records): Cupertino, CA
- FDA decisions: 6 (2000–2004): 6 510(k) clearances
- Product codes: DWF (6)
- 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
- K042156: Cardeon Cobra Catheter (Oct 6, 2004)
- K024058: Modification to Cardeon Aegis Catheter (Dec 30, 2002)
- K022042: Modification to Cardeon Ascending Balloon Cannula (Abc) (Sep 3, 2002)
- K022174: Modification to Cardeon Aegis Catheter (Jul 29, 2002)
- K013593: Cardeon Aegis Catheter (Jun 24, 2002)
- K001371: Cardeon Ascending Balloon Cannula (Abc) (Jul 7, 2000)

Source page: https://510kreport.com/company/cardeon