510(k) K860138 ยท DDB Ceruloplasmin, Antigen, Antiserum, Control
NO. 615 DETERMINATION OF CERULOPLASMIN IN SERUM
| Applicant | Sigma Diagnostics, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Mar 28, 1986 |
| Received | Jan 14, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860138
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.