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FDA 510(k) Applications Submitted by MELISSA 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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