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MAGNETOM VERIO

Page Type
Cleared 510(K)
510(k) Number
K072237
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2007
Days to Decision
58 days
Submission Type
Summary

MAGNETOM VERIO

Page Type
Cleared 510(K)
510(k) Number
K072237
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2007
Days to Decision
58 days
Submission Type
Summary