Honeywell Hommed, LLC
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K153719 | LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream | DRG | 2016-06-03 | View |
| 510(k) | K112858 | GENESIS TOUCH SYSTEM | DRG | 2012-01-24 | View |
| 510(k) | K101242 | GENESIS DM MODEL: 6053000A1 | DRG | 2010-06-11 | View |
| 510(k) | K072272 | HONEYWELL HOMMED CENTRAL STATION 4.0 | DXN | 2007-09-07 | View |
| 510(k) | K061087 | GENESIS OTC MONITOR | DRG | 2006-06-09 | View |
| 510(k) | K061088 | SENTRY OTC MONITOR | DRG | 2006-06-09 | View |
| 510(k) | K053453 | HOMMED CENTRAL STATION, VERSION 3.5 | DXN | 2006-05-05 | View |
No matching devices.
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