Lucas Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lucas Medical, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Lucas Medical, Inc. has 7 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Historical record: 7 cleared submissions from 1996 to 1999. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lucas Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lucas Medical, Inc.
7 devices
Cleared
Jul 30, 1999
LMI CAROTID ENDARTERECTOMY SHUNT CATHETER, MODEL #'S CES, CESR, CESB, CESRB,...
Cardiovascular
275d
Cleared
Nov 19, 1997
LMI IRRIGATION CATHETER (IGR)
Cardiovascular
128d
Cleared
Jul 01, 1997
LMI THROMBECTOMY CATHETER
Cardiovascular
130d
Cleared
May 10, 1996
LMI BILIARY CATHETER
Gastroenterology & Urology
183d
Cleared
Apr 11, 1996
LMI ARTERIAL EMBOLECTOMY CATHETER
Cardiovascular
177d
Cleared
Mar 11, 1996
LMI OCCLUSION CATHETER
Cardiovascular
123d
Cleared
Feb 28, 1996
LMI BILUMEN IRRIGATION ARTERIAL EMBOLECTOMY CAHTETER
Cardiovascular
89d