510(k) K893742 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
FILTRAL TM 20 HEMODIALYZER/FILTER
| Applicant | Hospal Medical Corp., Williamsburg VA, US |
| Decision | Substantially Equivalent, Jul 24, 1989 |
| Received | May 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893742
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.