FDA 510(k) Applications Submitted by ETHICON, INC

FDA 510(k) Number Submission Date Device Name Applicant
K173162 09/29/2017 GYNECARE TVT Abdominal Guides and Couplers, GYNECARE TVT Reuseable Introducer, GYNECARE TVT Reusable Rigid Catheter Guide Ethicon, Inc
K180829 03/30/2018 PROLENE Polypropylene Mesh Non-Absorbable Synthetic Surgical Mesh, PROLENE (Polypropylene) Hernia System, Non-absorbable Synthetic Surgical Mesh Ethicon, Inc


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