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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact