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ICAD BREAST INTERVENTIONAL PLANNING SOFTWARE, MODEL D70024

Page Type
Cleared 510(K)
510(k) Number
K090223
510(k) Type
Traditional
Applicant
ICAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2009
Days to Decision
60 days
Submission Type
Summary

ICAD BREAST INTERVENTIONAL PLANNING SOFTWARE, MODEL D70024

Page Type
Cleared 510(K)
510(k) Number
K090223
510(k) Type
Traditional
Applicant
ICAD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2009
Days to Decision
60 days
Submission Type
Summary