Larsen & Toubro Limited - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Larsen & Toubro Limited has 18 FDA 510(k) cleared cardiovascular devices. Based in Crofton, US.
Historical record: 18 cleared submissions from 2003 to 2011.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
18 devices
Cleared
Mar 15, 2011
STAR 50 N
Cardiovascular
88d
Cleared
Mar 11, 2011
STELLAR 300
Cardiovascular
78d
Cleared
Apr 29, 2010
STELLAR 300
Cardiovascular
212d
Cleared
Nov 20, 2009
SKYLINE 55, MODEL VER 1
Cardiovascular
127d
Cleared
Jun 05, 2009
STAR 55 MODEL 100
Cardiovascular
133d
Cleared
Jun 05, 2009
PLANET 55, MODEL 100
Cardiovascular
105d
Cleared
Sep 26, 2008
GALAXY 55
Cardiovascular
11d
Cleared
Jul 31, 2008
SKYLINE 55
Cardiovascular
58d
Cleared
Feb 08, 2008
STAR 55
Cardiovascular
15d
Cleared
Sep 21, 2007
PLANET 55
Cardiovascular
115d
Cleared
Jul 12, 2006
GALAXY
Cardiovascular
14d
Cleared
Jan 20, 2006
STELLAR 404T
Cardiovascular
11d