FDA 510(k) Applications Submitted by TOMMIE J MORGAN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040032	01/08/2004	CENTRAL STATION, VERSION 3.3H	HOMMED LLC.
K020184	01/18/2002	HOMMED CENTRAL STATION	HOMMED LLC.
K040651	03/11/2004	HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM	HOMMED LLC.
K040799	03/29/2004	HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS	HOMMED LLC.
K061087	04/18/2006	GENESIS OTC MONITOR	HONEYWELL HOMMED, LLC
K061088	04/18/2006	SENTRY OTC MONITOR	HONEYWELL HOMMED, LLC
K003180	10/11/2000	HOMMED OBSERVER, MODEL I	HOMMED LLC.
K014025	12/06/2001	HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER	HOMMED LLC.
K053453	12/12/2005	HOMMED CENTRAL STATION, VERSION 3.5	HONEYWELL HOMMED LLC
K004044	12/29/2000	HOMMED SENTRY III PATIENT MONITOR SYSTEM	HOMMED LLC.