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Fujifilm Sonosite Vevo MD Imaging System

Page Type
Cleared 510(K)
510(k) Number
K160674
510(k) Type
Traditional
Applicant
FUJIFILM SONOSITE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2016
Days to Decision
40 days
Submission Type
Summary

Fujifilm Sonosite Vevo MD Imaging System

Page Type
Cleared 510(K)
510(k) Number
K160674
510(k) Type
Traditional
Applicant
FUJIFILM SONOSITE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2016
Days to Decision
40 days
Submission Type
Summary