510(k) K791339 ยท DDB Ceruloplasmin, Antigen, Antiserum, Control
HUMAN CERULOPLASMIN
| Applicant | Beckman Instruments, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 16, 1979 |
| Received | Jul 16, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791339
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.