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SA 9900 PLUS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032329
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2003
Days to Decision
8 days
Submission Type
Summary

SA 9900 PLUS DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K032329
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2003
Days to Decision
8 days
Submission Type
Summary