FDA 510(k) Applications Submitted by Philips Medical System Nederland B.V.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K201081 | 04/22/2020 | AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter | Philips Medical System Nederland B.V. |
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