FDA 510(k) Applications Submitted by LeMaitre Vascular Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K110891 03/30/2011 THE UNBALLOON NON-OCCLUSIVE CATHETER; THE UNBALLOON NON-OCCLUSIVE MODELING CATHETER LEMAITRE VASCULAR INC.
K121839 06/22/2012 UNBALLOON NON-OCCLUSIVE MODELING CATHETER LEMAITRE VASCULAR INC.
K212894 09/10/2021 PhasTIPP LeMaitre Vascular Inc.
K183513 12/18/2018 XenoSure Dura Biologic Patch LeMaitre Vascular Inc.


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