Honeywell Hommed, LLC is one of 4785 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Honeywell Hommed, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Honeywell Hommed, LLC has 7 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 7 cleared submissions from 2006 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Honeywell Hommed, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Honeywell Hommed, LLC
7 devices
Cleared
Jun 03, 2016
LifeStream Management System, LifeStream Management Suite, LifeStream Patient...
Cardiovascular
158d
Cleared
Jan 24, 2012
GENESIS TOUCH SYSTEM
Cardiovascular
116d
Cleared
Jun 11, 2010
GENESIS DM MODEL: 6053000A1
Cardiovascular
39d
Cleared
Sep 07, 2007
HONEYWELL HOMMED CENTRAL STATION 4.0
Cardiovascular
23d
Cleared
Jun 09, 2006
GENESIS OTC MONITOR
Cardiovascular
52d
Cleared
Jun 09, 2006
SENTRY OTC MONITOR
Cardiovascular
52d
Cleared
May 05, 2006
HOMMED CENTRAL STATION, VERSION 3.5
Cardiovascular
144d