510(k) K782151 ยท FJI Dialyzer, Capillary, Hollow Fiber
ARTIFICIAL KIDNEY, C-DAK 0.6D
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 22, 1979 |
| Received | Dec 26, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782151
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.