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ACUSON ANTARES DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063803
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2007
Days to Decision
14 days
Submission Type
Summary

ACUSON ANTARES DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063803
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/5/2007
Days to Decision
14 days
Submission Type
Summary