FDA 510(k) Applications Submitted by TIMOTHY WADE

FDA 510(k) Number Submission Date Device Name Applicant
K131493 05/23/2013 SIDEKICK AND USHER SUPPORT CATHETERS C.R. BARD, INC.
K112308 08/11/2011 CROSSER RECANALIZATION SYSTEM C.R. BARD, INC.
K163420 12/06/2016 UltraScore Focused Force PTA Balloon BARD PERIPHERAL VASCULAR, INC.
K143522 12/12/2014 Presto Inflation Device C.R. BARD, INC.


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