# Vascon, LLC

- Location (FDA's records): Miami, FL
- FDA decisions: 4 (2004–2008): 4 510(k) clearances
- Product codes: DQY (3), KRA (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 24 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Alvimedica Tibbi Urunler Sanayi VE Dis Ticaret A.S: 1 (https://510kreport.com/company/alvimedica-tibbi-urunler-sanayi-ve-dis-ticaret-a-s)

## Its most-cited devices
- K043387: Vascon Polaris Guiding Catheter (2005), cited by 2
- K033633: Vascon Polaris Guiding Catheter (2004), cited by 1

## Recent decisions
- K053310: Vascon Roamer Microcatheter (Jul 3, 2008)
- K052004: Vascon Neuropath Guiding Catheter (Jan 19, 2006)
- K043387: Vascon Polaris Guiding Catheter (Feb 16, 2005)
- K033633: Vascon Polaris Guiding Catheter (Feb 18, 2004)

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