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FDA 510(k) Applications Submitted by Kristi Fox
FDA 510(k) Number
Submission Date
Device Name
Applicant
K191394
05/24/2019
ILLUMISITE Platform
Covidien llc
K111644
06/13/2011
MOBICATH TRANSSEPTAL NEEDLE
Greatbatch Medical
K101784
06/25/2010
MOBICATH BI-DIRECTIONAL GUIDING SHEATH MODEL 1000182-XXX
Greatbatch Medical
K102540
09/03/2010
PTFE PORTABLE INTRODUCER
Greatbatch Medical
K093023
09/29/2009
PTFE PEELABLE INTRODUCER
Greatbatch Medical
K173244
10/06/2017
superDimension Navigation System V7.2
Covidien LLC
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