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Ingenia 3.0T, Ingenia 3.0T CX, Ingenia Elition and MR 7700 with Distributed Multi Nudclei

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213516
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland, B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
3/3/2022
Days to Decision
120 days
Submission Type
Summary