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ACCUVIX V7 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060087
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
1/24/2006
Days to Decision
12 days
Submission Type
Summary

ACCUVIX V7 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K060087
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
1/24/2006
Days to Decision
12 days
Submission Type
Summary