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MAGNETOM Avanto, MAGNETOM Verio with software syngo MR E11D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181613
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2018
Days to Decision
140 days
Submission Type
Summary