# Js Vascular, Inc.

- Location (FDA's records): Orinda, CA
- FDA decisions: 1 (2003–2003): 1 510(k) clearance
- Product codes: DQX (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (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
- Advanced Cardiovascular Systems, Inc.: 2 (https://510kreport.com/company/advanced-cardiovascular-systems)
- Terumo Corp.: 1 (https://510kreport.com/company/terumo)
- Boston Scientific Corporation Northwest Technology: 1 (https://510kreport.com/company/boston-scientific-northwest-technology)
- Shiley, Inc.: 1 (https://510kreport.com/company/shiley)
- American Omni Medical, Inc.: 1 (https://510kreport.com/company/american-omni-medical)

## Firms that cite its devices most
- Asahi Intecc Co., Ltd.: 1 (https://510kreport.com/company/asahi-intecc)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)

## Its most-cited devices
- K032411: JS Vascular Guide Wire Vise/Torque Device (2003), cited by 2

## Recent decisions
- K032411: JS Vascular Guide Wire Vise/Torque Device (Oct 7, 2003)

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