510(k) K832547 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ULTRAFILTRATION CONTROLLER
| Applicant | Extracorporeal Medical Specialities, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jan 3, 1984 |
| Received | Aug 1, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832547
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.