# Guidant Cardiac and Vascular Surgery

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 7 (1997–2002): 7 510(k) clearances
- Product codes: DQY (2), DYB (2), DQO (1), DRE (1), JAA (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (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
- Cordis Corp.: 2 (https://510kreport.com/company/cordis)
- I.Z.I. Corp.: 1 (https://510kreport.com/company/izi)

## Firms that cite its devices most
- Edwards Lifesciences, LLC: 2 (https://510kreport.com/company/edwards-lifesciences)
- Medtronic Endovascular Innovations: 1 (https://510kreport.com/company/medtronic-endovascular-innovations)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- W. L. Gore & Associates, Inc.: 1 (https://510kreport.com/company/w-l-gore-associates)

## Its most-cited devices
- K003495: Ancure Lliac Balloon Catheter (2001), cited by 3
- K003889: Ancure Sheath Model # 40315, 40320, 40325 (2002), cited by 2

## Recent decisions
- K003889: Ancure Sheath Model # 40315, 40320, 40325 (Jan 24, 2002)
- K001694: Guidant Retriever Device (May 15, 2001)
- K003495: Ancure Lliac Balloon Catheter (Feb 7, 2001)
- K002676: Endovance Dualpass Tear-Away Sheath Introducer (Oct 30, 2000)
- K970470: Evt Expandable Sheath (Jul 31, 1997)
- K970469: Evt Angioscale Angiographic Catheter (May 8, 1997)
- K970608: Evt Marker Board (Apr 21, 1997)

Source page: https://510kreport.com/company/guidant-cardiac-and-vascular-surgery