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FDA 510(k) Applications Submitted by Linda L. Julia Davila
FDA 510(k) Number
Submission Date
Device Name
Applicant
K182586
09/20/2018
DLP Aortic Root Cannula, DLP Aortic Root Cannula with Vent Line, DLP Pressure Monitoring Extension Line Adapter, DLP Cardioplegia Adapter with Pressure Port
Medtronic, Inc.
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