510(k) K963203 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
BENTLEY QUICK-PRIME HEMOCONCENTRATOR WITH DURAFLO TREATMENT
| Applicant | Baxter Healthcare Corp, Santa Ana CA, US |
| Decision | Substantially Equivalent, Mar 25, 1997 |
| Received | Aug 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963203
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.