FDA 510(k) Applications Submitted by Philips Electronics Nederland B.V.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K171055 | 04/10/2017 | Philips BlueControl | Philips Electronics Nederland B.V. |
| K192259 | 08/21/2019 | Philips IntelliSite Pathology Solution | Philips Electronics Nederland B.V. |
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