Datex-Ohmeda Inc., A Division of Instrumentarium C
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K093886 | ENGSTROM CARESTATION, ENGSTROM PRO | CBK | 2010-05-03 | View |
| 510(k) | K092864 | AESPIRE 7900, AESPIRE VIEW | BSZ | 2010-01-12 | View |
No matching devices.
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