FDA 510(k) Applications Submitted by DAWN CHANG

FDA 510(k) Number Submission Date Device Name Applicant
K120431 02/13/2012 HALO90 ULTRA ABLATION CATHETER BARRX MEDICAL, INC.
K140553 03/04/2014 ENDOWRIST STAPLER 45 AND STAPLER 45 RELOADS INTUITIVE SURGICAL, INC.
K172510 08/21/2017 ╡Cor Heart Failure and Arrhythmia Management System ZOLL Manufacturing Corporation
K112454 08/25/2011 HALO60 ABLATION CATHETER BARRX MEDICAL, INC.
K083287 11/07/2008 AVIVO MOBILE PATIENT MANAGEMENT SYSTEM CORVENTIS, INC.


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