# Philips Volcano

- Location (FDA's records): San Diego, CA
- FDA decisions: 2 (2016–2017): 2 510(k) clearances
- Product codes: PDU (1), IYO (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 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
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)
- Volcano Corporation: 1 (https://510kreport.com/company/volcano)

## Firms that cite its devices most
- Volcano Corporation: 1 (https://510kreport.com/company/volcano)

## Its most-cited devices
- K170133: FFR V2.5 (2017), cited by 1

## Recent decisions
- K170133: FFR V2.5 (May 26, 2017)
- K162418: Pioneer Plus Catheter (Dec 2, 2016)

Source page: https://510kreport.com/company/philips-volcano