FDA 510(k) Applications Submitted by Philips Medizin Systeme B÷blingen GmbH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211900 | 06/21/2021 | Patient Information Center iX | Philips Medizin Systeme B÷blingen GmbH |
| K221348 | 05/09/2022 | IntelliVue Patient Monitor MX750 (866471);IntelliVue Patient Monitor MX850 (866470) | Philips Medizin Systeme B÷blingen GmbH |
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