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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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