FDA 510(k) Applications Submitted by DOUGLAS W WOODRUFF

FDA 510(k) Number	Submission Date	Device Name	Applicant
K070071	01/08/2007	OMNIGUIDE ZERO FLOW ZF-T WAVEGUIDE FIBER	OMNIGUIDE, INC.
K070157	01/17/2007	OMNIGUIDE BEAM PATH CO2 MARK III WAVEGUIDE FIBER	OMNIGUIDE, INC.
K081939	07/08/2008	OMNIGUIDE BEAMPATH FIBER OPTIC HANDPIECE SYSTEM AND STERILIZATION TRAY	OMNIGUIDE, INC.
K062423	08/18/2006	OMNIGUIDE BEAMPATH LASER BEAM DELIVERY SYSTEM	OMNIGUIDE, INC.
K063141	10/16/2006	OMNIGUIDE ZERO FLOW ZF-T 150 WAVEGUIDE FIBER	OMNIGUIDE, INC.
K093251	10/16/2009	OMNIGUIDE BEAMPATH FELS 25A CO2 LASER SYSTEM	OMNIGUIDE, INC.
K093451	11/05/2009	OMNIGUIDE BEAMPATH CO2 MARK III WAVEGUIDE FIBER WITH LOW PROFILE/LOW LOSS TIP	OMNIGUIDE, INC.
K073313	11/26/2007	MARK III WAVEGUIDE FIBER WITH LOW PROFILE TIP	OMNIGUIDE, INC.
K073409	12/04/2007	OMNIGUIDE STERILE WAVEGUIDE ADAPTER SYSTEM	OMNIGUIDE, INC.