FDA 510(k) Applications Submitted by PATRICIA LIAU

FDA 510(k) Number	Submission Date	Device Name	Applicant
K160734	03/17/2016	SonoSite SII Ultrasound System	FUJIFILM SonoSite, Inc.
K161119	04/20/2016	SonoSite iViz Ultrasound System	FUJIFILM SONOSITE,INC.
K142017	07/25/2014	X-PORTE ULTRASOUND SYSTEM	FUJIFILM SonoSite, Inc.
K152209	08/07/2015	FUJIFILM SonoSite X-Porte Ultrasound System	FUJIFILM SONOSITE,INC.
K162288	08/15/2016	SonoSite iViz Ultrasound System	FUJIFILM SONOSITE, INC.
K152983	10/09/2015	FUJIFILM SonoSite iViz Ultrasound System	FUJIFILM SONOSITE,INC.
K133454	11/12/2013	SONOSITE EDGE ULTRASOUND SYSTEM	FUJIFILM SONOSITE,INC.
K153626	12/18/2015	SonoSite Edge II Ultrasound System	FUJIFILM SONOSITE,INC.