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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