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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.
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