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Sertera Biopsy Device

Page Type
Cleared 510(K)
510(k) Number
K150169
510(k) Type
Traditional
Applicant
Hologic, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2015
Days to Decision
200 days
Submission Type
Summary

Sertera Biopsy Device

Page Type
Cleared 510(K)
510(k) Number
K150169
510(k) Type
Traditional
Applicant
Hologic, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2015
Days to Decision
200 days
Submission Type
Summary