FDA 510(k) Applications Submitted by RICHARD E GORDON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K092785	09/10/2009	COMBINED VASOMEDICAL-BIOX AMBULATORY ECG & BLOOD PRESSURE RECORDER & ANALYSIS SOFTWARE, 2301	VASOMEDICAL, INC.
K013888	11/23/2001	FIXATION (STEINMANN) PINS	MILTEX, INC.
K111096	04/20/2011	VASOMEDICAL-BIOX COMBINED 12 CHANNEL AMBULATORY ECG AND BLOOD PRESSURE RECORDER MODEL 2302, VASOMEDICAL-BIOX AMBULATORY	VASOMEDICAL, INC.
K111180	04/27/2011	VASOMEDICAL-BIOX 12- CHANNEL AMBULATORY ECG HOLTER RECORDER MODEL 1304, VASOMEDICAL-BIOX 3- CHANNEL MINIATURE AMBULATORY	VASOMEDICAL, INC.