510(k) K802831 ยท KPF System, Dialysate Delivery, Semi-Automatic, Peritoneal
GAMBRO PERITONEAL DIALYSIS MONITOR
| Applicant | Gambro, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 18, 1980 |
| Received | Nov 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802831
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.