Aloka Co. Ltd USA
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) | K041916 | ALOKA SSD-ALPHA 5 ULTRASOUND SYSTEM | IYN | 2004-07-30 | View |
| 510(k) | K032875 | ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM | IYO | 2003-09-30 | View |
No matching devices.
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