# Philips North America, LLC

- Location (FDA's records): Bothell, WA
- FDA decisions: 1 (2021–2021): 1 510(k) clearance
- Product codes: LDD (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
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)
- Physio-Control Corp.: 1 (https://510kreport.com/company/physio-control)

## Recent decisions
- K203231: Switched Internal Paddles (Jan 11, 2021)

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