510(k) K791584 ยท KPF System, Dialysate Delivery, Semi-Automatic, Peritoneal
CYLER/HEATER FOR PERITONEAL DIALYSIS
| Applicant | American Medical Products, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 16, 1979 |
| Received | Aug 17, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791584
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.