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MAMMOSITE CAVITY EVALUATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081179
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
14 days
Submission Type
Summary

MAMMOSITE CAVITY EVALUATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K081179
510(k) Type
Traditional
Applicant
HOLOGIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/2008
Days to Decision
14 days
Submission Type
Summary