FDA 510(k) Applications Submitted by Michelle Ragozzino 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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