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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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