# Trans Vascular Incorporated

- Location (FDA's records): Menlo Park, CA
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: ITX (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lumend, Inc.: 1 (https://510kreport.com/company/lumend)

## Firms that cite its devices most
- Medtronic, Inc.: 2 (https://510kreport.com/company/medtronic)

## Its most-cited devices
- K013363: Crosspoint Transaccess Catheter (2002), cited by 2
- K031920: Crosspoint Transaccess Catheter, Model TA-XP-001 (2003), cited by 1

## Recent decisions
- K031920: Crosspoint Transaccess Catheter, Model TA-XP-001 (Jul 23, 2003)
- K013363: Crosspoint Transaccess Catheter (Apr 2, 2002)

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