FDA 510(k) Applications Submitted by CONNIE WHITE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970461	02/06/1997	CELL ROBOTICS ER: YAG SURGICAL LASER	CELL ROBOTICS, INC.
K981746	05/18/1998	CELL ROBOTICS' LASETTE	CELL ROBOTICS, INC.
K963683	08/29/1996	TRU-PULSE LASER (MODIFIED)	TISSUE TECHNOLOGIES, INC.
K973431	09/10/1997	LASETTE	CELL ROBOTICS, INC.
K965124	12/23/1996	LASETTE	CELL ROBOTICS, INC.
K040563	03/03/2004	LS FAMILY OF CO2 LASERS INCLUDING: LS-15 LASER SYSTEM (15 WATT) AND LS-25 LASER SYSTEM (25 WATT)	SANDSTONE MEDICAL TECHNOLOGIES, LLC
K000929	03/22/2000	PROLITE PULSED LIGHT SYSTEM	MEDICAL BIO CARE SWEDEN AB
K041011	04/20/2004	ULTRALIGHT II ND:YAG LASER SYSTEM	SANDSTONE MEDICAL TECHNOLOGIES, LLC
K002072	07/07/2000	PROLITE VL PULSED LIGHT SYSTEM	MEDICAL BIO CARE SWEDEN AB
K022378	07/22/2002	PLASMALITE PULSED LIGHT SYSTEM	MEDICAL BIO CARE SWEDEN AB
K022568	08/02/2002	PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF UNWANTED HAIR	MEDICAL BIO CARE SWEDEN AB
K022569	08/02/2002	PROLITE/PLASMALITE MPX PULSED LIGHT SYSTEM FOR TREATMENT OF VASCULAR LESIONS	MEDICAL BIO CARE SWEDEN AB
K004021	12/27/2000	F1 DIODE LASER SYSTEM	OPUS MEDICAL, INC.
K010927	03/28/2001	MODIFICATION TO PROLITE PULSED LIGHT SYSTEM	MEDICAL BIO CARE SWEDEN AB
K010928	03/28/2001	PROLITE VL PULSED LIGHT SYSTEM	MEDICAL BIO CARE SWEDEN AB
K023081	09/17/2002	PROLITE / PLASMALITE MPX PULSED LIGHT SYSTEM (PERMANENT HAIR REDUCTION)	MEDICAL BIO CARE SWEDEN AB