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ACUSON S2000 AND S3000

Page Type
Cleared 510(K)
510(k) Number
K130881
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
196 days
Submission Type
Summary

ACUSON S2000 AND S3000

Page Type
Cleared 510(K)
510(k) Number
K130881
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/11/2013
Days to Decision
196 days
Submission Type
Summary