FDA 510(k) Applications Submitted by MELISSA C. SCHULTZ

FDA 510(k) Number Submission Date Device Name Applicant
K092064 07/08/2009 SOUNDSTAR 3D ULTRASOUND CATHETER, MODEL M-5723-12 BIOSENSE WEBSTER, INC.
K101138 04/22/2010 SOUNDSTAR 3D ULTRASOUND CATHETER MODEL M-5723-12 BIOSENSE WEBSTER, INC.
K161701 06/20/2016 CARTO ENT System BIOSENSE WEBSTER


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