# Arterial Vascular Engineering, Inc.

- Location (FDA's records): Billerica, MA
- FDA decisions: 3 (1997–1999): 3 510(k) clearances
- Product codes: FGE (1), DQO (1), DQT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 2 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medtronic, Inc.: 1 (https://510kreport.com/company/medtronic)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Neometrics, Inc.: 1 (https://510kreport.com/company/neometrics)
- Medtronic Inc. Cardiac Rhythm Management: 1 (https://510kreport.com/company/medtronic-cardiac-rhythm-management)

## Its most-cited devices
- K983927: GT1 Floppy, GT1 HI-Per Flex, GT1 Light Support (1999), cited by 4

## Recent decisions
- K984627: Ave 4F Siteseer Cardiovascular Angiographic Catheter (Jul 27, 1999)
- K983927: GT1 Floppy, GT1 HI-Per Flex, GT1 Light Support (Mar 11, 1999)
- K971295: Ave Bridge Stent System (Nov 5, 1997)

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