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FDA 510(k) Applications Submitted by Surge Cardiovascular
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170488
02/17/2017
Peak Left Ventricular Vent Cannula, 20 Fr.; Peak Left Ventricular Vent Cannula, 18 Fr; Peak Left Ventricular Vent Cannula, 16 Fr
Surge Cardiovascular
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