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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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