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ARCADIS AVANTIC

Page Type
Cleared 510(K)
510(k) Number
K051133
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2005
Days to Decision
29 days
Submission Type
Summary

ARCADIS AVANTIC

Page Type
Cleared 510(K)
510(k) Number
K051133
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2005
Days to Decision
29 days
Submission Type
Summary