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MAGNETOM Avantofit, MAGNETOM Skyrafit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162102
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2016
Days to Decision
116 days
Submission Type
Summary