# Philips Medical Systems Netherland BV

- Location (FDA's records): Best, NL
- FDA decisions: 1 (2014–2014): 1 510(k) clearance
- Product codes: OWB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 81 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Philips Medical Systems Nederland B.V.: 1 (https://510kreport.com/company/philips-medical-systems-nederland)

## Firms that cite its devices most
- Philips Medical Systems Nederland B.V.: 2 (https://510kreport.com/company/philips-medical-systems-nederland)
- Philips Medical Systems Nethrlands BV: 1 (https://510kreport.com/company/philips-medical-systems-nethrlands)

## Its most-cited devices
- K141979: Allura Xper FD Series / Allura Xper or Table Series (2014), cited by 3

## Recent decisions
- K141979: Allura Xper FD Series / Allura Xper or Table Series (Aug 19, 2014)

Source page: https://510kreport.com/company/philips-medical-systems-netherland