FDA 510(k) Applications Submitted by Nancy Burke

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110414	02/14/2011	QLAB 8.1 QUANTIFICATION SOFTWARE	PHILIPS ULTRASOUND, INC.
K080548	02/28/2008	HD7 DIAGNOSTIC ULTRASOUND SYSTEM	PHILLIPS MEDICAL SYSTEMS
K130684	03/13/2013	PHILIPS HEARTSTART FR3 AUTOMATED EXTERNAL DEFIBRILLATOR	PHILIPS MEDICAL SYSTEMS
K152369	08/21/2015	ACUSON S1000, S2000, S3000 Diagnostic Ultrasuond System	SIEMENS MEDICAL SOLUTIONS, USA, INC. ULTRASOUND GROUP
K142876	10/01/2014	ACUSON S1000/ S2000/ S3000 Diagnostic Ultrasound Systems	SIEMENS MEDICAL SOLUTIONS USA, INC.
K143254	11/13/2014	eSie Apps Suite	SIEMENS MEDICAL SOLUTIONS USA, INC.
K093563	11/18/2009	IU22 ULTRASOUND SYSTEM AND TRANSDUCERS	PHILIPS ULTRASOUND, INC.
K103815	12/29/2010	Q-STATION	PHILIPS ULTRASOUND, INC.