# Philips Image Guided Therapy Devices

- Location (FDA's records): Colorado Springs, CO
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: MJN (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 0 (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
- Qxmedical, LLC: 1 (https://510kreport.com/company/qxmedical)
- Spectranetics Corp.: 1 (https://510kreport.com/company/spectranetics)

## Recent decisions
- K251358: Bridge Plus Occlusion Balloon (590-002) (Jun 24, 2025)

Source page: https://510kreport.com/company/philips-image-guided-therapy-devices