FDA 510(k) Applications Submitted by XINTEC CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990914	03/18/1999	POLARIS DIODE LASER SYSTEM AND ACCESSORIES	XINTEC CORPORATION
K971065	03/24/1997	DENTICA PULSED ND: YAG LASER SYSTEMS AND ACCESSORIES	XINTEC CORPORATION
K971912	04/11/1997	PROTEGE ER:YAG LASER SYSTEM AND ACCESSORIES	XINTEC CORPORATION
K981350	04/14/1998	ALEXIS ALEXANDRITE LASER SYSTEM AND ACCESSORIES	XINTEC CORPORATION
K951876	04/21/1995	PROTEGE ER:YAG SURGICAL LASER SYSTEM AND ACCESSORIES	XINTEC CORPORATION
K951935	04/25/1995	PRODIGY SUPERPULSE ND:YAG SURGICAL LASER SYSTEMS & ACCESSORIES	XINTEC CORPORATION
K981627	05/07/1998	PROTEGE II ER: YAG LASER SYSTEM AND ACCESSOIES (UPGRADE)	XINTEC CORPORATION
K082230	08/07/2008	VECTRA PLUS LASER SYSTEM AND ACCESSORIES	XINTEC CORPORATION