FDA 510(k) Applications Submitted by Kim Kuan LEE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K180497	02/26/2018	Scone Mask	ResMed Ltd
K112489	08/29/2011	SWIFT FX BELLA	RESMED LTD.
K171212	04/25/2017	AirFit N20	ResMed Ltd
K161978	07/18/2016	AirFit N20	ResMed Ltd
K153673	12/21/2015	AirFit N20	ResMed Ltd
K070937	04/04/2007	MULTIPLE BRAND MALE LATEX CONDOM	NULATEX SDN. BHD.
K955706	12/15/1995	JPI AUTOMATIC X-RAY FILM PROCESSOR	JPI HEALTHCARE CO., LTD
K090872	03/30/2009	MODIFICATION TO CARDICA C-PORT XA DISTAL ANASTOMOSIS SYSTEM	CARDICA, INC.
K091017	04/09/2009	CARDICA PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM, MODEL FG-000001	CARDICA, INC.
K150372	02/13/2015	VERASENSE Knee System	OrthoSensor, Inc.
K130380	02/14/2013	ORTHOSENSOR KNEE BALANCER	ORTHOSENSOR, INC.