510(k) K802613 ยท FJI Dialyzer, Capillary, Hollow Fiber
C-PAK MODEL 12 ARTIFICIAL KIDNEY
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 7, 1981 |
| Received | Oct 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802613
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.