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SOFTWARE VERSION A2.5 FOR MAGNETOM 42SP/63SP SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924489
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/15/1993
Days to Decision
134 days
Submission Type
Summary