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ACUSON S3000, S2000 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K183575
510(k) Type
Traditional
Applicant
Siemens Healthineers
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2019
Days to Decision
89 days
Submission Type
Summary

ACUSON S3000, S2000 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K183575
510(k) Type
Traditional
Applicant
Siemens Healthineers
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2019
Days to Decision
89 days
Submission Type
Summary