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ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090334
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2009
Days to Decision
10 days
Submission Type
Summary

ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090334
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/20/2009
Days to Decision
10 days
Submission Type
Summary