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Trident HD Specimen Radiography System

Page Type
Cleared 510(K)
510(k) Number
K182727
510(k) Type
Traditional
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2019
Days to Decision
104 days
Submission Type
Summary

Trident HD Specimen Radiography System

Page Type
Cleared 510(K)
510(k) Number
K182727
510(k) Type
Traditional
Applicant
Hologic, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/10/2019
Days to Decision
104 days
Submission Type
Summary