FDA 510(k) Applications Submitted by Gert De Vries

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.
K192914 10/15/2019 Stimuplex Onvision System Philips Medical Systems Nederland B.V.


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