510(k) K013550 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
CLIRANS E-SERIES DIALYZER
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Nov 20, 2001 |
| Received | Oct 24, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K013550
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.