Trident HD Specimen Radiography System— 510(k) K182727

Substantially Equivalent

Hologic, Inc.

FDA 510(k) clearance K182727 for Trident HD Specimen Radiography System, Substantially Equivalent on 2019-01-10. Applicant: Hologic, Inc..

Clearance details

Applicant: Hologic, Inc.
Product code: Code MWP
Advisory panel: Radiology
Date received: 2018-09-28
Decision date: 2019-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danbury, CT, US

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