Honeywell Hommed, LLC
Houston, TX, US
Honeywell Hommed, LLC appears in FDA device records in Houston, TX. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Honeywell Hommed, LLC between 2006 and 2016. The busiest year on record is 2006, with 3. The most recent is 2016, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2006 | 3 |
| 2007 | 1 |
| 2010 | 1 |
| 2012 | 1 |
| 2014 | 1 |
| 2016 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K153719 | LifeStream Management System, LifeStream Management Suite, LifeStream Patient Manager, LifeStream Manager, LifeStream Web Manager, LifeStream | DRG | Substantially Equivalent | |
| K141792 | GENESIS TOUCH SYSTEM | DRG | Substantially Equivalent | |
| K112858 | GENESIS TOUCH SYSTEM | DRG | Substantially Equivalent | |
| K101242 | GENESIS DM MODEL: 6053000A1 | DRG | Substantially Equivalent | |
| K072272 | HONEYWELL HOMMED CENTRAL STATION 4.0 | DXN | Substantially Equivalent | |
| K061088 | SENTRY OTC MONITOR | DRG | Substantially Equivalent | |
| K061087 | GENESIS OTC MONITOR | DRG | Substantially Equivalent | |
| K053453 | HOMMED CENTRAL STATION, VERSION 3.5 | DXN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain