510(k) K853510 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
MINIFILTER HEMOFILTER
| Applicant | Amicon, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Sep 12, 1985 |
| Received | Aug 21, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853510
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.