510(k) K830284 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FH 101, FH 202 & FH 303 FIBER HEMOFILTER
| Applicant | Gambro, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 2, 1983 |
| Received | Jan 27, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830284
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.