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SONOACE 9900 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012867
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
16 days
Submission Type
Summary

SONOACE 9900 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K012867
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/2001
Days to Decision
16 days
Submission Type
Summary