FDA 510(k) Applications Submitted by REVERSE MEDICAL CORPORATION

FDA 510(k) Number	Submission Date	Device Name	Applicant
K110055	01/10/2011	REVERSE MEDICAL REFLEX GUIDE CATHETER	REVERSE MEDICAL CORPORATION
K091563	05/28/2009	RECRUIT MICROCATHETER	REVERSE MEDICAL CORPORATION
K102418	08/25/2010	REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM	REVERSE MEDICAL CORPORATION
K141313	05/20/2014	REVERSE MEDICAL MICRO VASCULAR PLUG SYSTEM	REVERSE MEDICAL CORPORATION
K130858	03/28/2013	REVERSE MEDICAL MICROCATHETER	REVERSE MEDICAL CORPORATION
K112262	08/08/2011	REFLEX BALLON GUIDE CATHETER	REVERSE MEDICAL CORPORATION
K122684	08/31/2012	REVERSE MEDICAL MICROCATHETER	REVERSE MEDICAL CORPORATION
K133282	10/25/2013	REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM	REVERSE MEDICAL CORPORATION
K123803	12/10/2012	REVERSE MEDICAL MICRO VASCULAR PLUG (MVP) SYSTEM	REVERSE MEDICAL CORPORATION
K150108	01/20/2015	Reverse Medical Micro Vascular Plug System	REVERSE MEDICAL CORPORATION