Edwards Lifesciences, LLC · Class II · Cleared Mar 13, 2013
| K-number | K123370 |
| Device name | EZ GLIDE AORTIC CANNULA, AORTIC PERFUSION CANNULA WITH DURAFLO COATING, DISPERSION AORTIC PERFUSION CANNULA |
| Applicant | Edwards Lifesciences, LLC |
| Product code | DWF |
| Device class | Class II |
| Decision date | Mar 13, 2013 |
| Decision | Substantially Equivalent |
| Regulation | 870.4210 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov