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FDA 510(k) Applications Submitted by Rachelle D. Fitzgerald
FDA 510(k) Number
Submission Date
Device Name
Applicant
K173822
12/18/2017
Anchor Tissue Retrieval System by CONMED
Conmed Corporation
K191281
05/13/2019
Omni Hysteroscope, Omni Lok cervical seal
Hologic, Inc.
K181974
07/24/2018
MyoSure XL Tissue Removal Device for Fluent
Hologic, Inc
K182006
07/27/2018
Omni Hysteroscope, Omni Hysteroscope Kits, Omni Sheaths
Hologic, Inc
K182052
07/31/2018
Omni Instrument Tray
Hologic, Inc
K172940
09/26/2017
ANCHOR Tissue Retrieval System
Conmed Corporation
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