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FUJIFILM Sonosite Vevo MD Imaging System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190476
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2019
Days to Decision
16 days
Submission Type
Summary

FUJIFILM Sonosite Vevo MD Imaging System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190476
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2019
Days to Decision
16 days
Submission Type
Summary