Honeywell Hommed, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Honeywell Hommed, LLC Cardiovascular ✕
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