510(k) K800330 ยท FKP System, Dialysate Delivery, Single Patient
MODEL 7200 HEMODIALYSIS DELIVERY SYSTEM
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Apr 8, 1980 |
| Received | Feb 13, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800330
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.