510(k) K800704 ยท FJI Dialyzer, Capillary, Hollow Fiber
C-DAK TM 2800 ARTIFICIAL KIDNEY
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 8, 1980 |
| Received | Mar 31, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800704
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.