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ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142876
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2014
Days to Decision
22 days
Submission Type
Summary

ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142876
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/23/2014
Days to Decision
22 days
Submission Type
Summary