Philips DS North America, LLC
Philips DS North America, LLC appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 5, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K250800 | UroNav 4 | June 5, 2025 |