Medtronic, Inc. · Class II · Cleared Oct 19, 2018
| K-number | K182586 |
| Device name | DLP Aortic Root Cannula, DLP Aortic Root Cannula with Vent Line, DLP Pressure Monitoring Extension Line Adapter, DLP Cardioplegia Adapter with Pressure Port |
| Applicant | Medtronic, Inc. |
| Product code | DWF |
| Device class | Class II |
| Decision date | Oct 19, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 870.4210 |
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