510(k) K923727 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
PRIMUS HOLLOW FIBER DIALYZER MOD. 1000, 1350, 2000
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 29, 1994 |
| Received | Jul 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923727
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.