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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