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ClearView cCAD

Page Type
Cleared 510(K)
510(k) Number
K161959
510(k) Type
Traditional
Applicant
ClearView Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2016
Days to Decision
163 days
Submission Type
Summary

ClearView cCAD

Page Type
Cleared 510(K)
510(k) Number
K161959
510(k) Type
Traditional
Applicant
ClearView Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2016
Days to Decision
163 days
Submission Type
Summary