Last synced on 14 November 2025 at 11:06 pm

SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000030
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2000
Days to Decision
14 days
Submission Type
Summary

SONOACE 600 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K000030
510(k) Type
Traditional
Applicant
MEDISON AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2000
Days to Decision
14 days
Submission Type
Summary