510(k) K182302 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
CardioGard Emboli Protection Cannula
| Applicant | Cardiogard Medical, Ltd., Or Yehuda, IL |
| Decision | Substantially Equivalent, May 17, 2019 |
| Received | Aug 24, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182302
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.