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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact