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ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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