# Philips Medical Systems MR Finland

- Location (FDA's records): Vantaa, FI
- FDA decisions: 4 (2008–2020): 4 510(k) clearances
- Product codes: MUJ (3), MOS (1)
- 510(k) review time since 2016: median 197 days, against 80 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 4 (2 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
- Mri Devices Corp.: 1 (https://510kreport.com/company/mri-devices)
- Philips Medical Systems (Cleveland), Inc.: 1 (https://510kreport.com/company/philips-medical-systems-cleveland)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)

## Firms that cite its devices most
- Philips OY: 1 (https://510kreport.com/company/philips)
- Spectronic Medical AB: 1 (https://510kreport.com/company/spectronic-medical)

## Its most-cited devices
- K193109: MRCAT brain (2020), cited by 2
- K151435: MRCAT (2016), cited by 1
- K182888: MRCAT Pelvis (2019), cited by 1

## Recent decisions
- K193109: MRCAT brain (Jan 24, 2020)
- K182888: MRCAT Pelvis (Apr 30, 2019)
- K151435: MRCAT (Feb 25, 2016)
- K080120: Hfo Shoulder Coil (Mar 10, 2008)

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