510(k) K973322 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
DIAPACT CRRT
| Applicant | B.Braun Medical, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Nov 10, 1998 |
| Received | Sep 4, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973322
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.