FDA 510(k) Applications Submitted by JENNIFER KIMBALL

FDA 510(k) Number Submission Date Device Name Applicant
K060323 02/09/2006 ULTRAFLEX PRECISION COLONIC STENT, MODELS M00557330, MO00557360, M00557380 Boston Scientific Corporation
K092009 07/06/2009 MODIFICATION TO: LEVEEN SUPERSLIM NEEDLE ELECTRODES, MODELS M001262260, M001262270, M001262280, M001262290 Boston Scientific Corporation


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