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SOFTWARE SYNGO MR D13A FOR THE MAGNETOM SYSTEMS AERA/SKYRA/AVANTO/VERIO

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121434
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/2012
Days to Decision
175 days
Submission Type
Summary