FDA 510(k) Applications Submitted by Philips Medical Systems Nederland, B.V.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K213516 | 11/03/2021 | Ingenia 3.0T, Ingenia 3.0T CX, Ingenia Elition and MR 7700 with Distributed Multi Nudclei | Philips Medical Systems Nederland, B.V. |
| K210760 | 03/15/2021 | Precise Image | Philips Medical Systems Nederland, B.V. |
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