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SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013627
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
11 days
Submission Type
Summary

SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013627
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2001
Days to Decision
11 days
Submission Type
Summary