FDA 510(k) Applications Submitted by VASCUTECH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K980723 02/24/1998 2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT) VASCUTECH, INC.
K001621 05/26/2000 DARDIK CAROTID SHUNT VASCUTECH, INC.
K992368 07/15/1999 LEMAITRE EMBOLECTOMY CATHETER VASCUTECH, INC.
K992933 08/31/1999 LEMAITRE IRRIGATION CATHETER VASCUTECH, INC.
K992934 08/31/1999 LEMAITRE VENOUS THROMBECTOMY CATHETER VASCUTECH, INC.
K992940 08/31/1999 LEMAITRE BALLOON CATHETER WITH IRRIGATION VASCUTECH, INC.
K992941 08/31/1999 LEMAITRE BILIARY CATHETER VASCUTECH, INC.
K992942 08/31/1999 LEMAITRE OCCLUSION CATHETER VASCUTECH, INC.


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