FDA 510(k) Applications Submitted by LAURA HEATON

FDA 510(k) Number Submission Date Device Name Applicant
K100063 01/11/2010 HYPERFORM OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER, HYPERGLIDE OCCLUSION BALLOON CATHETER MODEL EV3 INC
K150108 01/20/2015 Reverse Medical Micro Vascular Plug System REVERSE MEDICAL CORPORATION
K113455 11/21/2011 SOLITAIRE FR REVASCULARIZATION DEVICE MICRO THERAPEUTICS DBA EV3 NEUROVASCULAR
K093750 12/07/2009 ECHELON MICRO CATHETER, MARATHON MICRO CATHETER, NAUTICA MICRO CATHETER ULTRAFLOW HPC FLOW DIRECTED MICRO CATHETER, REBA EV3 INC


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