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ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K092159
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/28/2009
Days to Decision
12 days
Submission Type
Summary

ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K092159
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/28/2009
Days to Decision
12 days
Submission Type
Summary