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FDA 510(k) Applications Submitted by Michelle Ragozzine Rodgers
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140438
02/21/2014
MICRO GUIDE CATHETER ELITE
CORDIS CORP., A JOHNSON & JOHNSON CO.
K150836
03/30/2015
OUTBACK Elite Re-Entry Catheter
CORDIS CORPORATION, A JOHNSON & JOHNSON CO.
K180081
01/11/2018
RAILWAY Sheathless Access System
Cordis Corporation
K150187
01/27/2015
ELITECROSS Support Catheter
Cordis Corporation, A Johnson & Johnson Company
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