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FUJIFILM FC1 Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K160406
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2016
Days to Decision
29 days
Submission Type
Summary

FUJIFILM FC1 Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K160406
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/2016
Days to Decision
29 days
Submission Type
Summary