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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