Hommed, LLC
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K040799 | HOMMED GENESIS PATIENT MONITOR SYSTEM WITH OPTIONS | DXN | 2004-08-18 | View |
| 510(k) | K040651 | HOMMED SENTRY IIIB-F PATIENT MONITOR SYSTEM | DXN | 2004-08-10 | View |
| 510(k) | K040032 | CENTRAL STATION, VERSION 3.3H | DXN | 2004-02-27 | View |
| 510(k) | K020184 | HOMMED CENTRAL STATION | DXN | 2002-04-22 | View |
| 510(k) | K014025 | HOMMED SENTRY III PATIENT MONITOR SYSTEM WITH CARD READER | DQA | 2002-04-09 | View |
| 510(k) | K003180 | HOMMED OBSERVER, MODEL I | DXN | 2001-06-28 | View |
| 510(k) | K004044 | HOMMED SENTRY III PATIENT MONITOR SYSTEM | DQA | 2001-03-02 | View |
| 510(k) | K993938 | THE HOMMED SENTRY, MODEL 1 SENTRY | DXN | 2000-03-15 | View |
No matching devices.
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