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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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