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SonoSite X-Porte Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K171437
510(k) Type
Traditional
Applicant
FujiFilm SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2017
Days to Decision
27 days
Submission Type
Summary

SonoSite X-Porte Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K171437
510(k) Type
Traditional
Applicant
FujiFilm SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2017
Days to Decision
27 days
Submission Type
Summary