FDA 510(k) Applications Submitted by MARY ROSE

FDA 510(k) Number	Submission Date	Device Name	Applicant
K090398	02/17/2009	PROVENT PROFESSIONAL SLEEP APNEA THERAPY	VENTUS MEDICAL, INC.
K051041	04/25/2005	INSULIN PUMP	ABBOTT DIABETES CARE INC.
K171332	05/08/2017	Artemis Neuro Evacuation Device	Penumbra, Inc.
K102397	08/24/2010	KYPHON XPEDE BONE CEMENT	Medtronic
K062770	09/15/2006	COPILOT HEALTH MANAGEMENT SYSTEM	ABBOTT DIABETES CARE INC.
K152699	09/21/2015	Apollo System	PENUMBRA, INC.
K183296	11/27/2018	REAL Immersive System	Penumbra, Inc.
K093828	12/14/2009	KYPH X HV-R BONE CEMENT	MEDTRONIC INC.
K123902	12/18/2012	PHYSICAL MONITORING REGISTRATION UNIT-S (PMRU-S)	OKTX LLC
K002104	07/12/2000	COMBINED PHYSIOLOGICAL MONITORING SYSTEM	MARYROSE CUSIMANO, PH.D. & SCOTT ZEFF
K022719	08/15/2002	PHYSICAL MONITORING REGISTRATION UNIT	MARYROSE CUSIMANO, PH.D./PHIL REASTON