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MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081121
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2008
Days to Decision
44 days
Submission Type
Summary

MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081121
510(k) Type
Traditional
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC., ULTRASOUND DI
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2008
Days to Decision
44 days
Submission Type
Summary