Vascutech, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Vascutech, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Washington, US.
Historical record: 14 cleared submissions from 1985 to 2000.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Dec 06, 2000
DARDIK CAROTID SHUNT
Cardiovascular
194d
Cleared
Apr 13, 2000
LEMAITRE OCCLUSION CATHETER
Cardiovascular
226d
Cleared
Mar 08, 2000
LEMAITRE IRRIGATION CATHETER
Cardiovascular
190d
Cleared
Mar 01, 2000
LEMAITRE VENOUS THROMBECTOMY CATHETER
Cardiovascular
183d
Cleared
Feb 22, 2000
LEMAITRE BALLOON CATHETER WITH IRRIGATION
Cardiovascular
175d
Cleared
Jan 12, 2000
LEMAITRE BILIARY CATHETER
Gastroenterology & Urology
134d
Cleared
Dec 09, 1999
LEMAITRE EMBOLECTOMY CATHETER
Cardiovascular
147d
Cleared
Feb 12, 1999
2.0MM EXPANDABLE LEMAITRE VALVULOTOME (ELV 2.0- GNT)
Cardiovascular
353d
Cleared
Jun 21, 1995
LEMAITRE VALVULOTOME II
Cardiovascular
173d
Cleared
Sep 21, 1993
THE SAMUELS RETROGRAD VALVULOTOME
Cardiovascular
151d
Cleared
Jul 22, 1993
STERILE LEMAITRE GLOW 'N TELL TAPE
Radiology
78d
Cleared
Feb 16, 1993
LEMAITRE RETROGRADE VALVULOTOME
Cardiovascular
182d
Cleared
Sep 18, 1991
LEMAITRE-BOOKWALTER VESSEL DEVICES
Cardiovascular
100d
Cleared
Apr 24, 1985
LEMAITRE RETROGRADE VALVULOTOME-MANU-SURGICA INSTR
Cardiovascular
82d