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Vascutech, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K001621DARDIK CAROTID SHUNTDecember 6, 2000
K992942LEMAITRE OCCLUSION CATHETERApril 13, 2000
K992933LEMAITRE IRRIGATION CATHETERMarch 8, 2000
K992934LEMAITRE VENOUS THROMBECTOMY CATHETERMarch 1, 2000
K992940LEMAITRE BALLOON CATHETER WITH IRRIGATIONFebruary 22, 2000
K992941LEMAITRE BILIARY CATHETERJanuary 12, 2000
K992368LEMAITRE EMBOLECTOMY CATHETERDecember 9, 1999
K9807232.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT)February 12, 1999
K946352LEMAITRE VALVULOTOME IIJune 21, 1995
K932009THE SAMUELS RETROGRAD VALVULOTOMESeptember 21, 1993
K932184STERILE LEMAITRE GLOW 'N TELL TAPEJuly 22, 1993
K924171LEMAITRE RETROGRADE VALVULOTOMEFebruary 16, 1993
K912548LEMAITRE-BOOKWALTER VESSEL DEVICESSeptember 18, 1991
K850394LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTRApril 24, 1985