510(k) K790565 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
AORTIC ROOT CANNULA
| Applicant | Dlp, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 11, 1979 |
| Received | Mar 19, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790565
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Nov 4, 2024 | Medtronic Perfusion Systems Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012; for use in cardiopulmonary bypass surgery Open, Classified |
DWF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.