FDA 510(k) Applications Submitted by MARY MELLOWS

FDA 510(k) Number Submission Date Device Name Applicant
K151659 06/19/2015 ReliaTack Articulating Reloadable Fixation Device with Deep Purchase Reloadable Tacks Covidien LLC
K142547 09/10/2014 Bluntport Blunt Trocar with Threaded Anchor 5mm-12mm COVIDIEN
K122781 09/11/2012 RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
K142656 09/18/2014 Surgical Gut Suture COVIDIEN


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