Philips Electronics Nederland B.V.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2019-09-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K192259 | Philips IntelliSite Pathology Solution | PSY | 2019-09-20 | View |
| 510(k) | K171055 | Philips BlueControl | ONE | 2017-07-06 | View |
No matching devices.