510(k) K923312 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
HIGH PERMEABILITY DIALYER
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Feb 18, 1994 |
| Received | Jul 7, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923312
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.