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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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