510(k) K131935 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ELISIO-H HEMODIALYZER, ELISIO-M HEMODIALYZER
| Applicant | Nipro Medical Corporation, Miami FL, US |
| Decision | Substantially Equivalent, Dec 20, 2013 |
| Received | Jun 27, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131935
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.