510(k) K170574 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
Diacap Pro Dialyzer
| Applicant | B. Braun Avitum AG, Melsungen, DE |
| Decision | Substantially Equivalent, Aug 11, 2017 |
| Received | Feb 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170574
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.