510(k) K131381 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ELISIO-H HEMODIALYZER
| Applicant | Nipro Medical Corporation, Suwanee GA, US |
| Decision | Substantially Equivalent, Dec 19, 2013 |
| Received | May 14, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131381
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.