510(k) K874020 ยท KPF System, Dialysate Delivery, Semi-Automatic, Peritoneal
ULTRACARE(TM) AUTOMATED PATIENT ASSIST DEVICE
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Jan 29, 1988 |
| Received | Oct 2, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874020
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.