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MODIFICATION TO ACUSON ANTARES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063138
510(k) Type
Special
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2006
Days to Decision
37 days
Submission Type
Summary

MODIFICATION TO ACUSON ANTARES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063138
510(k) Type
Special
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2006
Days to Decision
37 days
Submission Type
Summary