FDA 510(k) Applications Submitted by Meghan Wakeford

FDA 510(k) Number Submission Date Device Name Applicant
K190694 03/18/2019 Unifi Workspace v1.0.0 Hologic, Inc.
K240886 04/01/2024 Fluent Pro Fluid Management System (FLT-200); Fluent Pro Fluid Management System Disposable Procedure Kit (6-pack) (FLT-212); Fluent Pro Fluid Management System Disposable Procedure Kit (1-pack) (FLT-212S); Fluent Pro Fluid Management System Tissue Trap M Hologic, Inc.
K182727 09/28/2018 Trident HD Specimen Radiography System Hologic, Inc.


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