FDA 510(k) Applications Submitted by LARSEN & TOUBRO LIMITED

FDA 510(k) Number	Submission Date	Device Name	Applicant
K081552	06/03/2008	SKYLINE 55	LARSEN & TOUBRO LIMITED
K040409	02/18/2004	LARSEN & TOUBRO LIMITED SENORITA COLOR DOPPLER ULTRASOUND SYSTEM	LARSEN & TOUBRO LIMITED
K103686	12/17/2010	STAR 50 N	LARSEN & TOUBRO LIMITED
K051608	06/17/2005	STAR 50 MONITORING SYSTEM	LARSEN & TOUBRO LIMITED
K032867	09/15/2003	STAR (LUNAR SERIES) MONITORING SYSTEM	LARSEN & TOUBRO LIMITED
K032871	09/15/2003	PLANET MONITORING SYSTEM	LARSEN & TOUBRO LIMITED
K093017	09/29/2009	STELLAR 300	LARSEN & TOUBRO LIMITED
K043370	12/08/2004	PLANET 50 MONITORING SYSTEM	LARSEN & TOUBRO LIMITED
K103763	12/23/2010	STELLAR 300	LARSEN & TOUBRO LIMITED
K060058	01/09/2006	STELLAR 404T	LARSEN & TOUBRO LIMITED
K042560	09/21/2004	STELLAR 404 MONITORING SYSTEM	LARSEN & TOUBRO LIMITED
K071472	05/29/2007	PLANET 55	LARSEN & TOUBRO LIMITED
K061816	06/28/2006	GALAXY	LARSEN & TOUBRO LIMITED
K090172	01/23/2009	STAR 55 MODEL 100	LARSEN & TOUBRO LIMITED
K080173	01/24/2008	STAR 55	LARSEN & TOUBRO LIMITED
K082685	09/15/2008	GALAXY 55	LARSEN & TOUBRO LIMITED
K092153	07/16/2009	SKYLINE 55, MODEL VER 1	LARSEN & TOUBRO LIMITED
K090443	02/20/2009	PLANET 55, MODEL 100	LARSEN & TOUBRO LIMITED