FDA 510(k) Applications Submitted by HONEYWELL HOMMED, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K112858 |
09/30/2011 |
GENESIS TOUCH SYSTEM |
HONEYWELL HOMMED, LLC |
K101242 |
05/03/2010 |
GENESIS DM MODEL: 6053000A1 |
HONEYWELL HOMMED, LLC |
K153719 |
12/28/2015 |
LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream |
HONEYWELL HOMMED, LLC |
K072272 |
08/15/2007 |
HONEYWELL HOMMED CENTRAL STATION 4.0 |
HONEYWELL HOMMED, LLC |
K061087 |
04/18/2006 |
GENESIS OTC MONITOR |
HONEYWELL HOMMED, LLC |
K061088 |
04/18/2006 |
SENTRY OTC MONITOR |
HONEYWELL HOMMED, LLC |
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