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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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