510(k) K123288 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
HEMOCONCENTRATOR
| Applicant | Maquet Cardiopulmonary, AG, Rastatt De-Bw, DE |
| Decision | Substantially Equivalent, Jun 26, 2013 |
| Received | Oct 22, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123288
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.