Cardiosonix, Ltd.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| QUANTIX OR VESSEL STABILIZER DEVICE (K041180) | Cardiosonix, Ltd. | 2004-06-07 |
| QUANTIX/OR DEVICE (K030357) | Cardiosonix, Ltd. | 2003-08-20 |
| QUANTIX/ND DEVICE (K023431) | Cardiosonix, Ltd. | 2002-11-13 |
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