510(k) K802893 ยท FJI Dialyzer, Capillary, Hollow Fiber
CORDIS DOW C-DAK 1.3MRC ARTIF. KIDNEY
| Applicant | Cordis Corp., Walker MI, US |
| Decision | Substantially Equivalent, Feb 13, 1981 |
| Received | Nov 17, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802893
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.