Philips Electronics Nederland B.V.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K192259 | Philips IntelliSite Pathology Solution | September 20, 2019 |
| K171055 | Philips BlueControl | July 6, 2017 |