Cardiosonix, Ltd.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K041180 | QUANTIX OR VESSEL STABILIZER DEVICE | DPW | 2004-06-07 | View |
| 510(k) | K030357 | QUANTIX/OR DEVICE | DPW | 2003-08-20 | View |
| 510(k) | K023431 | QUANTIX/ND DEVICE | DPW | 2002-11-13 | View |
No matching devices.
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