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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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