# Abbott Vascular Devices

- Location (FDA's records): Redwood, CA
- FDA decisions: 4 (1994–2005): 2 510(k) clearances and 2 original PMA approvals
- Product codes: NTE (1), FGE (1), MGB (1), LOX (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)
- Abbott Laboratories: 1 (https://510kreport.com/company/abbott-laboratories)

## Firms that cite its devices most
- Abbott Vascular-Vascular Solutions: 2 (https://510kreport.com/company/abbott-vascular-vascular-solutions)
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K052454: The Emboshield Embolic Protection System (2005), cited by 2
- K050501: Modification to: Xceed Nitinol Self-Expanding Transhepatic Biliary Stent System (2005), cited by 1

## Recent decisions
- P050007: Starclose Vascular Closure System (Dec 21, 2005)
- K052454: The Emboshield Embolic Protection System (Sep 14, 2005)
- K050501: Modification to: Xceed Nitinol Self-Expanding Transhepatic Biliary Stent System (Mar 14, 2005)
- P910031: Oracle (TM) Coronary Balloon Dilatation Catheter (Sep 30, 1994)

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