510(k) K914363 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
PERITONEAL DIALYSIS CYCLER SET
| Applicant | National Medical Care, Medical Products Div., Inc., Rockleigh NJ, US |
| Decision | Substantially Equivalent, Mar 16, 1992 |
| Received | Oct 1, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914363
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.