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ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082142
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2008
Days to Decision
106 days
Submission Type
Summary

ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082142
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2008
Days to Decision
106 days
Submission Type
Summary