FDA 510(k) Applications Submitted by RUOJUAN ZHANG

FDA 510(k) Number Submission Date Device Name Applicant
K162931 10/19/2016 Ingenia 1.5T CX and Ingenia 3.0T CX R5.3 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
K163116 11/07/2016 Ingenia 1.5T, Ingenia 1.5T S and Ingenia 3.0T R5.3 Philips Medical Systems Nederland B.V.
K133819 12/16/2013 VERADIUS PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.


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