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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)
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

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

Page Type
Cleared 510(K)
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