# Philips Medical System Nederland B.V.

- Location (FDA's records): Best, NL
- FDA decisions: 1 (2020–2020): 1 510(k) clearance
- Product codes: DQK (1)
- Predicates its devices cite: 3 (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
- Ashitaka Factory of Terumo Corp.: 2 (https://510kreport.com/company/ashitaka-factory-of-terumo)
- St Jude Medical: 1 (https://510kreport.com/company/st-jude-medical)

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

## Its most-cited devices
- K201081: AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter (2020), cited by 1

## Recent decisions
- K201081: AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter (Dec 17, 2020)

Source page: https://510kreport.com/company/philips-medical-system-nederland