510(k) K823881 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
ARTERIOVENOUS BLOOD TUBING SET FOR
| Applicant | Amicon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1983 |
| Received | Dec 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823881
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.