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Ingenia 1.5T, Ingenia 1.5T S and Ingenia 3.0T R5.3

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163116
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
1/6/2017
Days to Decision
60 days
Submission Type
Summary