510(k) K171610 ยท PZS Dual Lumen Ecmo Cannula
MC3 QuickFlow Dual Lumen Catheter
| Applicant | Mc3 Incorporated, Dexter MI, US |
| Decision | Substantially Equivalent, Nov 16, 2017 |
| Received | Jun 1, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171610
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.