# Vascular Architects, Inc.

- Location (FDA's records): San Jose, CA
- FDA decisions: 5 (2001–2003): 5 510(k) clearances
- Product codes: JCT (3), ESW (1), DWX (1)
- Predicates its devices cite: 5 (5 its own); citations of its devices by later devices: 12 (5 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Alveolus, Inc.: 6 (https://510kreport.com/company/alveolus)
- Endarx, Inc.: 1 (https://510kreport.com/company/endarx)

## Its most-cited devices
- K003173: Aspire Covered Stent and Delivery Catheter (2001), cited by 5
- K012544: Vascular Architects Aspire Covered Stent and Controlled Expansion Delivery System (2001), cited by 5
- K030567: Modification to Vascular Architects Aspire Covered Stent and Contrilled Expansion Delivery System (2003), cited by 1
- K003719: Vascular Architects Periscope Device (2001), cited by 1

## Recent decisions
- K031641: Vascular Architects Aspire Covered Stent and 718 Delivery System (Aug 1, 2003)
- K030567: Modification to Vascular Architects Aspire Covered Stent and Contrilled Expansion Delivery System (Mar 24, 2003)
- K012544: Vascular Architects Aspire Covered Stent and Controlled Expansion Delivery System (Nov 15, 2001)
- K003173: Aspire Covered Stent and Delivery Catheter (Mar 13, 2001)
- K003719: Vascular Architects Periscope Device (Feb 28, 2001)

Source page: https://510kreport.com/company/vascular-architects