General Electric Company
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) | K110798 | SENOGRAPHE DS, SENOGRAPHE ESSENTIAL | MUE | 2011-12-22 | View |
| 510(k) | K103485 | SENOGRAPH DS, SENOGRAPH ESSENSTIAL | MUE | 2011-10-06 | View |
No matching devices.
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