# Bard Peripheral Vacular, Inc.

- Location (FDA's records): Tempe, AZ
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: PDU (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Firms that cite its devices most
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)

## Its most-cited devices
- K161208: CROSSER CTO Recanalization Catheter (2016), cited by 1

## Recent decisions
- K161208: CROSSER CTO Recanalization Catheter (May 24, 2016)

Source page: https://510kreport.com/company/bard-peripheral-vacular