ClearanceBrief
Company ยท US

Honeywell Hommed, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2016. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DRGTransmitters And Receivers, Physiological Signal, Radiofrequency6
DXNSystem, Measurement, Blood-Pressure, Non-Invasive2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 3, 2016K153719LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream We
Honeywell Hommed, LLC
DRG
Nov 25, 2014K141792GENESIS TOUCH SYSTEM
Honeywell Hommed
DRG
Jan 24, 2012K112858GENESIS TOUCH SYSTEM
Honeywell Hommed, LLC
DRG
Jun 11, 2010K101242GENESIS DM MODEL: 6053000A1
Honeywell Hommed, LLC
DRG
Sep 7, 2007K072272HONEYWELL HOMMED CENTRAL STATION 4.0
Honeywell Hommed, LLC
DXN
Jun 9, 2006K061088SENTRY OTC MONITOR
Honeywell Hommed, LLC
DRG
Jun 9, 2006K061087GENESIS OTC MONITOR
Honeywell Hommed, LLC
DRG
May 5, 2006K053453HOMMED CENTRAL STATION, VERSION 3.5
Honeywell Hommed, LLC
DXN

Latest recalls

DateFirm and productCodeLinked 510(k)
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