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Ingenia 1.5T, Ingenia 1 5T S, Ingenia 1.5T CX, Ingenia 3.0T CX R5.4

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
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510(k) Number
K173079
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/4/2018
Days to Decision
187 days
Submission Type
Summary