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SONOVIEW PRO BY MEDISON CO., LTD.

Page Type
Cleared 510(K)
510(k) Number
K031886
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2003
Days to Decision
12 days
Submission Type
Summary

SONOVIEW PRO BY MEDISON CO., LTD.

Page Type
Cleared 510(K)
510(k) Number
K031886
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/2003
Days to Decision
12 days
Submission Type
Summary