510(k) K071298 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
HF JUNIOR HEMOFILTER
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Aug 8, 2007 |
| Received | May 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071298
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.