Medtronic, Inc. · Class II · Cleared Jul 25, 2012
| K-number | K120988 |
| Device name | DLP SINGLE STAGE VENOUS CANNULA, DLP RIGHT ANGLE SINGLE STAGE VENOUS CANNULA, DLP SINGLE STAGE VENOUS CANNULA WITH RIGHT |
| Applicant | Medtronic, Inc. |
| Product code | DWF |
| Device class | Class II |
| Decision date | Jul 25, 2012 |
| Decision | Substantially Equivalent |
| Regulation | 870.4210 |
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