FDA 510(k) Applications Submitted by THOMAS BECZE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000023	01/04/2000	FRIENDLY LIGHT ER:YAG PULSED LASER	INNOTECH USA, INC.
K960552	02/08/1996	KNIGHT LIGHT NONLUBRICATED CONDOM	GLOBAL PROTECTION CORP.
K120672	03/05/2012	KD-936 FULLY AUTOMATIC WIRELESS BLOOD PRESSURE MONITOR	ANDON HEALTH CO.,LTD
K030739	03/10/2003	INFUSION DYNAMICS (ID) POWER INFUSER, MODEL M100B-3A WITH BLOOD CARTRIDGE	INFUSION DYNAMICS, INC.
K981489	04/27/1998	UROSURGE SPIRASTENT PLUS URETERAL STENT	UROSURGE, INC.
K981491	04/27/1998	UROSURGE FILASTENT URETERAL STENT	UROSURGE, INC.
K972158	06/09/1997	GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES	PRINCETON REGULATORY ASSOC.
K992044	06/17/1999	INFUSION DYNAMICS POWER INFUSER MODEL M100B	INFUSION DYNAMICS, INC.
K962770	07/16/1996	UROSURGE ACUTRAINER	PRINCETON REGULATORY ASSOC.
K973504	09/16/1997	UROSURGE UROSTENT	PRINCETON REGULATORY ASSOC.
K974074	10/29/1997	INFUSION DYNAMICS POWER INFUSER	INFUSION DYNAMICS, INC.
K965136	12/23/1996	UROSURGE UROTHERM FLUID WARMING SYSTEM	PRINCETON REGULATORY ASSOC.