FDA 510(k) Applications Submitted by REINHARD THIEME

FDA 510(k) Number	Submission Date	Device Name	Applicant
K060455	02/22/2006	MULTISTAR	ASCLEPION LASER TECHNOLOGIES GMBH
K060457	02/22/2006	QUADROSTAR 532	ASCLEPION LASER TECHNOLOGIES GMBH
K060459	02/22/2006	QUADROSTAR 980	ASCLEPION LASER TECHNOLOGIES GMBH
K060787	03/23/2006	TATTOOSTAR FAMILY	ASCLEPION LASER TECHNOLOGIES GMBH
K050900	04/11/2005	MEDIOSTAR XT	ASCLEPION LASER TECHNOLOGIES GMBH