FDA 510(k) Applications Submitted by BIOSENSE WEBSTER

FDA 510(k) Number Submission Date Device Name Applicant
K192397 09/03/2019 TruDi Navigation System Biosense Webster
K140318 02/10/2014 SOUNDSTAR ECO 8F GULTRASOUND CATHETER, SOUNDSTAR ECO 8F ULTRASOUND CATHETER BIOSENSE WEBSTER
K161701 06/20/2016 CARTO ENT System BIOSENSE WEBSTER


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