510(k) K203409 ยท PZS Dual Lumen Ecmo Cannula
MC3 Crescent Jugular Dual Lumen Catheter
| Applicant | Mc3, Inc., Dexter MI, US |
| Decision | Substantially Equivalent, May 3, 2021 |
| Received | Nov 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K203409
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.