Last synced on 17 May 2024 at 11:06 pm

Ingenia, Ingenia CX, Ingenia Elition, Ingenia Ambition, MR 5300 and MR 7700 MR Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223458
510(k) Type
Abbreviated
Applicant
Philips Medical Systems Nederland B.V.
Country
Netherlands
FDA Decision
Substantially Equivalent
Decision Date
4/6/2023
Days to Decision
141 days
Submission Type
Summary