FDA 510(k) Applications Submitted by CARDIOSONIX, LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030357 | 02/03/2003 | QUANTIX/OR DEVICE | CARDIOSONIX, LTD. |
| K041180 | 05/06/2004 | QUANTIX OR VESSEL STABILIZER DEVICE | CARDIOSONIX, LTD. |
| K023431 | 10/15/2002 | QUANTIX/ND DEVICE | CARDIOSONIX, LTD. |
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