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ECHELON Synergy MRI system

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223426
510(k) Type
Traditional
Applicant
FUJIFILM Healthcare Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/13/2023
Days to Decision
241 days
Submission Type
Summary