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SonoSite SII Ultrasound System, SonoSite Edge II Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K162045
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2016
Days to Decision
24 days
Submission Type
Summary

SonoSite SII Ultrasound System, SonoSite Edge II Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K162045
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/2016
Days to Decision
24 days
Submission Type
Summary