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ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080800
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
4/7/2008
Days to Decision
17 days
Submission Type
Summary

ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K080800
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
4/7/2008
Days to Decision
17 days
Submission Type
Summary