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VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003525
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2000
Days to Decision
7 days
Submission Type
Summary

VOLUSON 730 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003525
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2000
Days to Decision
7 days
Submission Type
Summary